ENST00000261937.11:c.3922G>T
MANE Select
|
ENSP00000261937.6:p.Val1308Leu
|
|
ENST00000261937.10:c.3922G>T
|
ENSP00000261937.6:p.Val1308Leu
|
|
ENST00000502603.5:n.622G>T
|
|
|
NM_182925.4:c.3922G>T
|
NP_891555.2:p.Val1308Leu
|
|
XM_011534477.1:c.4171G>T
|
XP_011532779.1:p.Val1391Leu
|
|
XM_011534478.1:c.4153G>T
|
XP_011532780.1:p.Val1385Leu
|
|
XM_011534479.1:c.*68G>T
|
XP_011532781.1:n.*68G>T
|
|
XM_011534482.1:c.3940G>T
|
XP_011532784.1:p.Val1314Leu
|
|
XM_011534483.1:c.3862G>T
|
XP_011532785.1:p.Val1288Leu
|
|
XM_011534484.1:c.3463G>T
|
XP_011532786.1:p.Val1155Leu
|
|
XR_941095.1:n.4208G>T
|
|
|
XM_011534478.3:c.4153G>T
|
XP_011532780.1:p.Val1385Leu
|
|
XM_011534484.2:c.3463G>T
|
XP_011532786.1:p.Val1155Leu
|
|
XM_017009263.1:c.*68G>T
|
XP_016864752.1:n.*68G>T
|
|
XM_017009268.1:c.3844G>T
|
XP_016864757.1:p.Val1282Leu
|
|
XR_001742050.2:n.4412G>T
|
|
|
NM_182925.5:c.3922G>T
MANE Select
|
NP_891555.2:p.Val1308Leu
|
|