ENST00000597188.6:c.3242T>C
MANE Select
|
ENSP00000471851.1:p.Val1081Ala
|
|
ENST00000270328.8:c.3242T>C
|
ENSP00000270328.4:p.Val1081Ala
|
|
ENST00000593913.5:c.*2119T>C
|
ENSP00000469901.1:n.*2119T>C
|
|
ENST00000595838.5:c.1703T>C
|
ENSP00000470501.1:p.Val568Ala
|
|
ENST00000597188.5:c.3242T>C
|
ENSP00000471851.1:p.Val1081Ala
|
|
NM_001282352.1:c.1703T>C
|
NP_001269281.1:p.Val568Ala
|
|
NM_030957.3:c.3242T>C
|
NP_112219.3:p.Val1081Ala
|
|
XM_006722917.2:c.2285T>C
|
XP_006722980.1:p.Val762Ala
|
|
XM_011528331.1:c.3389T>C
|
XP_011526633.1:p.Val1130Ala
|
|
XM_011528332.1:c.3389T>C
|
XP_011526634.1:p.Val1130Ala
|
|
XM_011528333.1:c.3389T>C
|
XP_011526635.1:p.Val1130Ala
|
|
XM_011528334.1:c.3065T>C
|
XP_011526636.1:p.Val1022Ala
|
|
XM_011528335.1:c.1958T>C
|
XP_011526637.1:p.Val653Ala
|
|
XM_011528336.1:c.1952T>C
|
XP_011526638.1:p.Val651Ala
|
|
XM_006722917.3:c.2285T>C
|
XP_006722980.1:p.Val762Ala
|
|
XM_017027338.2:c.3242T>C
|
XP_016882827.1:p.Val1081Ala
|
|
XM_017027339.1:c.1811T>C
|
XP_016882828.1:p.Val604Ala
|
|
XM_017027340.1:c.1805T>C
|
XP_016882829.1:p.Val602Ala
|
|
NM_030957.4:c.3242T>C
MANE Select
|
NP_112219.3:p.Val1081Ala
|
|
NM_001282352.2:c.1703T>C
|
NP_001269281.1:p.Val568Ala
|
|