ENST00000251127.11:c.3866T>C
MANE Select
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ENSP00000251127.6:p.Val1289Ala
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ENST00000648359.1:c.3866T>C
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ENSP00000497465.1:p.Val1289Ala
|
|
ENST00000675150.1:c.3587T>C
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ENSP00000502680.1:p.Val1196Ala
|
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ENST00000675332.1:c.3953T>C
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ENSP00000501955.1:p.Val1318Ala
|
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ENST00000676315.1:c.3779T>C
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ENSP00000501603.1:p.Val1260Ala
|
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ENST00000251127.10:c.3866T>C
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ENSP00000251127.6:p.Val1289Ala
|
|
NM_052867.2:c.3866T>C
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NP_443099.1:p.Val1289Ala
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XM_011521067.1:c.3923T>C
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XP_011519369.1:p.Val1308Ala
|
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XM_011521068.1:c.3866T>C
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XP_011519370.1:p.Val1289Ala
|
|
XM_011521069.1:c.3836T>C
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XP_011519371.1:p.Val1279Ala
|
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XM_011521070.1:c.3644T>C
|
XP_011519372.1:p.Val1215Ala
|
|
NM_001350748.1:c.3953T>C
|
NP_001337677.1:p.Val1318Ala
|
|
NM_001350749.1:c.3866T>C
|
NP_001337678.1:p.Val1289Ala
|
|
NM_001350750.1:c.3779T>C
|
NP_001337679.1:p.Val1260Ala
|
|
NM_001350751.1:c.3779T>C
|
NP_001337680.1:p.Val1260Ala
|
|
NM_052867.3:c.3866T>C
|
NP_443099.1:p.Val1289Ala
|
|
XM_011521067.2:c.3923T>C
|
XP_011519369.1:p.Val1308Ala
|
|
XM_011521069.2:c.3836T>C
|
XP_011519371.1:p.Val1279Ala
|
|
XM_017020536.2:c.3419T>C
|
XP_016876025.1:p.Val1140Ala
|
|
XM_017020537.1:c.3101T>C
|
XP_016876026.1:p.Val1034Ala
|
|
XM_024449336.1:c.4010T>C
|
XP_024305104.1:p.Val1337Ala
|
|
NM_052867.4:c.3866T>C
MANE Select
|
NP_443099.1:p.Val1289Ala
|
|
NM_001350748.2:c.3953T>C
|
NP_001337677.1:p.Val1318Ala
|
|
NM_001350749.2:c.3866T>C
|
NP_001337678.1:p.Val1289Ala
|
|
NM_001350750.2:c.3779T>C
|
NP_001337679.1:p.Val1260Ala
|
|
NM_001350751.2:c.3779T>C
|
NP_001337680.1:p.Val1260Ala
|
|