ENST00000306010.8:c.536T>C
|
ENSP00000302111.7:p.Val179Ala
|
|
ENST00000651593.1:c.443T>C
MANE Select
|
ENSP00000498729.1:p.Val148Ala
|
|
ENST00000306010.7:c.536T>C
|
ENSP00000302111.7:p.Val179Ala
|
|
NM_002412.3:c.536T>C
|
NP_002403.2:p.Val179Ala
|
|
NM_002412.4:c.536T>C
|
NP_002403.2:p.Val179Ala
|
|
XM_005252682.2:c.443T>C
|
XP_005252739.1:p.Val148Ala
|
|
XM_006717863.2:c.266T>C
|
XP_006717926.1:p.Val89Ala
|
|
XM_011539817.1:c.452T>C
|
XP_011538119.1:p.Val151Ala
|
|
NM_002412.5:c.443T>C
MANE Select
|
NP_002403.3:p.Val148Ala
|
|
XM_017016275.1:c.266T>C
|
XP_016871764.1:p.Val89Ala
|
|