ENST00000324071.10:c.992T>C
MANE Select
|
ENSP00000324648.2:p.Val331Ala
|
|
ENST00000598834.2:c.1016T>C
|
|
|
ENST00000324071.8:c.992T>C
|
ENSP00000324648.2:p.Val331Ala
|
|
ENST00000593831.1:c.284T>C
|
ENSP00000470582.1:p.Val95Ala
|
|
ENST00000597612.1:n.487T>C
|
|
|
NM_000767.4:c.992T>C
|
NP_000758.1:p.Val331Ala
|
|
XM_005258569.3:c.992T>C
|
XP_005258626.1:p.Val331Ala
|
|
XM_006723050.2:c.992T>C
|
XP_006723113.1:p.Val331Ala
|
|
XM_011526546.1:c.992T>C
|
XP_011524848.1:p.Val331Ala
|
|
XM_011526547.1:c.992T>C
|
XP_011524849.1:p.Val331Ala
|
|
XM_011526548.1:c.512T>C
|
XP_011524850.1:p.Val171Ala
|
|
XM_011526549.1:c.401T>C
|
XP_011524851.1:p.Val134Ala
|
|
XM_011526550.1:c.392T>C
|
XP_011524852.1:p.Val131Ala
|
|
NM_000767.5:c.992T>C
MANE Select
|
NP_000758.1:p.Val331Ala
|
|