ENST00000261937.11:c.3982G>T
MANE Select
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ENSP00000261937.6:p.Gly1328Ter
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ENST00000261937.10:c.3982G>T
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ENSP00000261937.6:p.Gly1328Ter
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|
ENST00000502603.5:n.682G>T
|
|
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NM_182925.4:c.3982G>T
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NP_891555.2:p.Gly1328Ter
|
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XM_011534477.1:c.4231G>T
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XP_011532779.1:p.Gly1411Ter
|
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XM_011534478.1:c.4213G>T
|
XP_011532780.1:p.Gly1405Ter
|
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XM_011534482.1:c.4000G>T
|
XP_011532784.1:p.Gly1334Ter
|
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XM_011534483.1:c.3922G>T
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XP_011532785.1:p.Gly1308Ter
|
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XM_011534484.1:c.3523G>T
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XP_011532786.1:p.Gly1175Ter
|
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XR_941095.1:n.4268G>T
|
|
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XM_011534478.3:c.4213G>T
|
XP_011532780.1:p.Gly1405Ter
|
|
XM_011534484.2:c.3523G>T
|
XP_011532786.1:p.Gly1175Ter
|
|
XM_017009263.1:c.*128G>T
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XP_016864752.1:n.*128G>T
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XM_017009268.1:c.3904G>T
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XP_016864757.1:p.Gly1302Ter
|
|
XR_001742050.2:n.4472G>T
|
|
|
NM_182925.5:c.3982G>T
MANE Select
|
NP_891555.2:p.Gly1328Ter
|
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