ENST00000261937.11:c.4076C>A
MANE Select
|
ENSP00000261937.6:p.Thr1359Lys
|
|
ENST00000261937.10:c.4076C>A
|
ENSP00000261937.6:p.Thr1359Lys
|
|
ENST00000502603.5:n.776C>A
|
|
|
NM_182925.4:c.4076C>A
|
NP_891555.2:p.Thr1359Lys
|
|
XM_011534477.1:c.4325C>A
|
XP_011532779.1:p.Thr1442Lys
|
|
XM_011534478.1:c.4307C>A
|
XP_011532780.1:p.Thr1436Lys
|
|
XM_011534482.1:c.4094C>A
|
XP_011532784.1:p.Thr1365Lys
|
|
XM_011534483.1:c.4016C>A
|
XP_011532785.1:p.Thr1339Lys
|
|
XM_011534484.1:c.3617C>A
|
XP_011532786.1:p.Thr1206Lys
|
|
XR_941095.1:n.4362C>A
|
|
|
XM_011534478.3:c.4307C>A
|
XP_011532780.1:p.Thr1436Lys
|
|
XM_011534484.2:c.3617C>A
|
XP_011532786.1:p.Thr1206Lys
|
|
XM_017009263.1:c.*222C>A
|
XP_016864752.1:n.*222C>A
|
|
XM_017009268.1:c.3998C>A
|
XP_016864757.1:p.Thr1333Lys
|
|
XR_001742050.2:n.4566C>A
|
|
|
NM_182925.5:c.4076C>A
MANE Select
|
NP_891555.2:p.Thr1359Lys
|
|