ENST00000261937.11:c.3905C>A
MANE Select
|
ENSP00000261937.6:p.Pro1302His
|
|
ENST00000261937.10:c.3905C>A
|
ENSP00000261937.6:p.Pro1302His
|
|
ENST00000502603.5:n.605C>A
|
|
|
NM_182925.4:c.3905C>A
|
NP_891555.2:p.Pro1302His
|
|
XM_011534477.1:c.4154C>A
|
XP_011532779.1:p.Pro1385His
|
|
XM_011534478.1:c.4136C>A
|
XP_011532780.1:p.Pro1379His
|
|
XM_011534479.1:c.*51C>A
|
XP_011532781.1:n.*51C>A
|
|
XM_011534482.1:c.3923C>A
|
XP_011532784.1:p.Pro1308His
|
|
XM_011534483.1:c.3845C>A
|
XP_011532785.1:p.Pro1282His
|
|
XM_011534484.1:c.3446C>A
|
XP_011532786.1:p.Pro1149His
|
|
XR_941095.1:n.4191C>A
|
|
|
XM_011534478.3:c.4136C>A
|
XP_011532780.1:p.Pro1379His
|
|
XM_011534484.2:c.3446C>A
|
XP_011532786.1:p.Pro1149His
|
|
XM_017009263.1:c.*51C>A
|
XP_016864752.1:n.*51C>A
|
|
XM_017009268.1:c.3827C>A
|
XP_016864757.1:p.Pro1276His
|
|
XR_001742050.2:n.4395C>A
|
|
|
NM_182925.5:c.3905C>A
MANE Select
|
NP_891555.2:p.Pro1302His
|
|