ENST00000356839.10:c.1277C>T
MANE Select
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ENSP00000349297.5:p.Ala426Val
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ENST00000322910.9:c.*1232C>T
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ENSP00000325395.5:n.*1232C>T
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ENST00000350303.9:c.1211C>T
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ENSP00000344152.5:p.Ala404Val
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ENST00000356839.9:c.1277C>T
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ENSP00000349297.5:p.Ala426Val
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ENST00000542255.6:c.135C>T
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ENST00000543245.6:c.1346C>T
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ENSP00000438689.2:p.Ala449Val
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ENST00000578579.2:n.448C>T
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|
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ENST00000578711.1:n.316C>T
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|
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ENST00000578824.5:n.693C>T
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ENST00000579425.5:n.301C>T
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ENST00000579546.1:c.114C>T
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ENST00000583850.5:n.52C>T
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ENST00000583858.5:c.306C>T
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|
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ENST00000585203.6:n.485C>T
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|
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NM_000018.3:c.1277C>T
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NP_000009.1:p.Ala426Val
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NM_001033859.2:c.1211C>T
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NP_001029031.1:p.Ala404Val
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|
NM_001270447.1:c.1346C>T
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NP_001257376.1:p.Ala449Val
|
|
NM_001270448.1:c.1049C>T
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NP_001257377.1:p.Ala350Val
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|
XM_006721516.2:c.1277C>T
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XP_006721579.2:p.Ala426Val
|
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XM_011523829.1:c.1277C>T
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XP_011522131.1:p.Ala426Val
|
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XM_011523830.1:c.1277C>T
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XP_011522132.1:p.Ala426Val
|
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XR_934021.1:n.1384C>T
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XR_934022.1:n.1384C>T
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|
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XR_934023.1:n.1384C>T
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XM_006721516.3:c.1277C>T
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XP_006721579.2:p.Ala426Val
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XM_011523829.2:c.1277C>T
|
XP_011522131.1:p.Ala426Val
|
|
XM_011523830.2:c.1277C>T
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XP_011522132.1:p.Ala426Val
|
|
XM_024450741.1:c.1277C>T
|
XP_024306509.1:p.Ala426Val
|
|
XR_934021.2:n.1336C>T
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XR_934022.2:n.1336C>T
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XR_934023.2:n.1336C>T
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NM_000018.4:c.1277C>T
MANE Select
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NP_000009.1:p.Ala426Val
|
|
NM_001033859.3:c.1211C>T
|
NP_001029031.1:p.Ala404Val
|
|
NM_001270447.2:c.1346C>T
|
NP_001257376.1:p.Ala449Val
|
|
NM_001270448.2:c.1049C>T
|
NP_001257377.1:p.Ala350Val
|
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