ENST00000379370.7:c.1807G>T
MANE Select
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ENSP00000368678.2:p.Gly603Ter
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ENST00000651234.1:c.1492G>T
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ENSP00000499046.1:p.Gly498Ter
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ENST00000652369.1:c.1492G>T
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ENSP00000498543.1:p.Gly498Ter
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ENST00000379370.6:c.1807G>T
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ENSP00000368678.2:p.Gly603Ter
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ENST00000620552.4:c.1393G>T
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ENSP00000484607.1:p.Gly465Ter
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NM_001305275.1:c.1807G>T
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NP_001292204.1:p.Gly603Ter
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NM_198576.3:c.1807G>T
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NP_940978.2:p.Gly603Ter
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XM_005244749.2:c.1807G>T
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XP_005244806.1:p.Gly603Ter
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XM_006710635.2:c.1807G>T
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XP_006710698.1:p.Gly603Ter
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XM_011541429.1:c.1807G>T
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XP_011539731.1:p.Gly603Ter
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XM_011541430.1:c.934G>T
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XP_011539732.1:p.Gly312Ter
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XM_011541431.1:c.73G>T
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XP_011539733.1:p.Gly25Ter
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XR_946650.1:n.1874G>T
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NM_001364727.1:c.1492G>T
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NP_001351656.1:p.Gly498Ter
|
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XM_005244749.3:c.1807G>T
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XP_005244806.1:p.Gly603Ter
|
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XM_011541429.2:c.1807G>T
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XP_011539731.1:p.Gly603Ter
|
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XR_946650.2:n.1878G>T
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NM_001305275.2:c.1807G>T
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NP_001292204.1:p.Gly603Ter
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NM_198576.4:c.1807G>T
MANE Select
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NP_940978.2:p.Gly603Ter
|
|
NM_001364727.2:c.1492G>T
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NP_001351656.1:p.Gly498Ter
|
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