ENST00000379370.7:c.1817T>C
MANE Select
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ENSP00000368678.2:p.Val606Ala
|
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ENST00000651234.1:c.1502T>C
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ENSP00000499046.1:p.Val501Ala
|
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ENST00000652369.1:c.1502T>C
|
ENSP00000498543.1:p.Val501Ala
|
|
ENST00000379370.6:c.1817T>C
|
ENSP00000368678.2:p.Val606Ala
|
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ENST00000620552.4:c.1403T>C
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ENSP00000484607.1:p.Val468Ala
|
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NM_001305275.1:c.1817T>C
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NP_001292204.1:p.Val606Ala
|
|
NM_198576.3:c.1817T>C
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NP_940978.2:p.Val606Ala
|
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XM_005244749.2:c.1817T>C
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XP_005244806.1:p.Val606Ala
|
|
XM_006710635.2:c.1817T>C
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XP_006710698.1:p.Val606Ala
|
|
XM_011541429.1:c.1817T>C
|
XP_011539731.1:p.Val606Ala
|
|
XM_011541430.1:c.944T>C
|
XP_011539732.1:p.Val315Ala
|
|
XM_011541431.1:c.83T>C
|
XP_011539733.1:p.Val28Ala
|
|
XR_946650.1:n.1884T>C
|
|
|
NM_001364727.1:c.1502T>C
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NP_001351656.1:p.Val501Ala
|
|
XM_005244749.3:c.1817T>C
|
XP_005244806.1:p.Val606Ala
|
|
XM_011541429.2:c.1817T>C
|
XP_011539731.1:p.Val606Ala
|
|
XR_946650.2:n.1888T>C
|
|
|
NM_001305275.2:c.1817T>C
|
NP_001292204.1:p.Val606Ala
|
|
NM_198576.4:c.1817T>C
MANE Select
|
NP_940978.2:p.Val606Ala
|
|
NM_001364727.2:c.1502T>C
|
NP_001351656.1:p.Val501Ala
|
|