ENST00000261937.11:c.3924G>A
MANE Select
|
ENSP00000261937.6:p.Val1308=
|
|
ENST00000261937.10:c.3924G>A
|
ENSP00000261937.6:p.Val1308=
|
|
ENST00000502603.5:n.624G>A
|
|
|
NM_182925.4:c.3924G>A
|
NP_891555.2:p.Val1308=
|
|
XM_011534477.1:c.4173G>A
|
XP_011532779.1:p.Val1391=
|
|
XM_011534478.1:c.4155G>A
|
XP_011532780.1:p.Val1385=
|
|
XM_011534479.1:c.*70G>A
|
XP_011532781.1:n.*70G>A
|
|
XM_011534482.1:c.3942G>A
|
XP_011532784.1:p.Val1314=
|
|
XM_011534483.1:c.3864G>A
|
XP_011532785.1:p.Val1288=
|
|
XM_011534484.1:c.3465G>A
|
XP_011532786.1:p.Val1155=
|
|
XR_941095.1:n.4210G>A
|
|
|
XM_011534478.3:c.4155G>A
|
XP_011532780.1:p.Val1385=
|
|
XM_011534484.2:c.3465G>A
|
XP_011532786.1:p.Val1155=
|
|
XM_017009263.1:c.*70G>A
|
XP_016864752.1:n.*70G>A
|
|
XM_017009268.1:c.3846G>A
|
XP_016864757.1:p.Val1282=
|
|
XR_001742050.2:n.4414G>A
|
|
|
NM_182925.5:c.3924G>A
MANE Select
|
NP_891555.2:p.Val1308=
|
|