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ENST00000356839.10:c.1205C=
MANE Select
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ENSP00000349297.5:p.Ala402=
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ENST00000322910.9:c.*1160C=
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ENSP00000325395.5:n.*1160C=
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ENST00000350303.9:c.1139C=
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ENSP00000344152.5:p.Ala380=
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ENST00000356839.9:c.1205C=
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ENSP00000349297.5:p.Ala402=
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ENST00000542255.6:c.63C=
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ENST00000543245.6:c.1274C=
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ENSP00000438689.2:p.Ala425=
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ENST00000578579.2:n.376C=
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ENST00000578711.1:n.162C=
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ENST00000578824.5:n.621C=
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ENST00000579425.5:n.229C=
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ENST00000579546.1:c.42C=
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ENST00000583858.5:c.234C=
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|
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ENST00000585203.6:n.413C=
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NM_000018.3:c.1205C=
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NP_000009.1:p.Ala402=
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NM_001033859.2:c.1139C=
|
NP_001029031.1:p.Ala380=
|
|
|
NM_001270447.1:c.1274C=
|
NP_001257376.1:p.Ala425=
|
|
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NM_001270448.1:c.977C=
|
NP_001257377.1:p.Ala326=
|
|
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XM_006721516.2:c.1205C=
|
XP_006721579.2:p.Ala402=
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|
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XM_011523829.1:c.1205C=
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XP_011522131.1:p.Ala402=
|
|
|
XM_011523830.1:c.1205C=
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XP_011522132.1:p.Ala402=
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|
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XR_934021.1:n.1312C=
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XR_934022.1:n.1312C=
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XR_934023.1:n.1312C=
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XM_006721516.3:c.1205C=
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XP_006721579.2:p.Ala402=
|
|
|
XM_011523829.2:c.1205C=
|
XP_011522131.1:p.Ala402=
|
|
|
XM_011523830.2:c.1205C=
|
XP_011522132.1:p.Ala402=
|
|
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XM_024450741.1:c.1205C=
|
XP_024306509.1:p.Ala402=
|
|
|
XR_934021.2:n.1264C=
|
|
|
|
XR_934022.2:n.1264C=
|
|
|
|
XR_934023.2:n.1264C=
|
|
|
|
NM_000018.4:c.1205C=
MANE Select
|
NP_000009.1:p.Ala402=
|
|
|
NM_001033859.3:c.1139C=
|
NP_001029031.1:p.Ala380=
|
|
|
NM_001270447.2:c.1274C=
|
NP_001257376.1:p.Ala425=
|
|
|
NM_001270448.2:c.977C=
|
NP_001257377.1:p.Ala326=
|
|
