ENST00000356839.10:c.902G>A
MANE Select
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ENSP00000349297.5:p.Gly301Asp
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ENST00000322910.9:c.*857G>A
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ENSP00000325395.5:n.*857G>A
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ENST00000350303.9:c.836G>A
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ENSP00000344152.5:p.Gly279Asp
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ENST00000356839.9:c.902G>A
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ENSP00000349297.5:p.Gly301Asp
|
|
ENST00000543245.6:c.971G>A
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ENSP00000438689.2:p.Gly324Asp
|
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ENST00000578824.5:n.51G>A
|
|
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ENST00000581378.5:c.620G>A
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|
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ENST00000582379.1:n.286G>A
|
|
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NM_000018.3:c.902G>A
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NP_000009.1:p.Gly301Asp
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NM_001033859.2:c.836G>A
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NP_001029031.1:p.Gly279Asp
|
|
NM_001270447.1:c.971G>A
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NP_001257376.1:p.Gly324Asp
|
|
NM_001270448.1:c.674G>A
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NP_001257377.1:p.Gly225Asp
|
|
XM_006721516.2:c.902G>A
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XP_006721579.2:p.Gly301Asp
|
|
XM_011523829.1:c.902G>A
|
XP_011522131.1:p.Gly301Asp
|
|
XM_011523830.1:c.902G>A
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XP_011522132.1:p.Gly301Asp
|
|
XR_934021.1:n.1009G>A
|
|
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XR_934022.1:n.1009G>A
|
|
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XR_934023.1:n.1009G>A
|
|
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XM_006721516.3:c.902G>A
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XP_006721579.2:p.Gly301Asp
|
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XM_011523829.2:c.902G>A
|
XP_011522131.1:p.Gly301Asp
|
|
XM_011523830.2:c.902G>A
|
XP_011522132.1:p.Gly301Asp
|
|
XM_024450741.1:c.902G>A
|
XP_024306509.1:p.Gly301Asp
|
|
XR_934021.2:n.961G>A
|
|
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XR_934022.2:n.961G>A
|
|
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XR_934023.2:n.961G>A
|
|
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NM_000018.4:c.902G>A
MANE Select
|
NP_000009.1:p.Gly301Asp
|
|
NM_001033859.3:c.836G>A
|
NP_001029031.1:p.Gly279Asp
|
|
NM_001270447.2:c.971G>A
|
NP_001257376.1:p.Gly324Asp
|
|
NM_001270448.2:c.674G>A
|
NP_001257377.1:p.Gly225Asp
|
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