ENST00000261937.11:c.4041C>T
MANE Select
|
ENSP00000261937.6:p.Asp1347=
|
|
ENST00000261937.10:c.4041C>T
|
ENSP00000261937.6:p.Asp1347=
|
|
ENST00000502603.5:n.741C>T
|
|
|
NM_182925.4:c.4041C>T
|
NP_891555.2:p.Asp1347=
|
|
XM_011534477.1:c.4290C>T
|
XP_011532779.1:p.Asp1430=
|
|
XM_011534478.1:c.4272C>T
|
XP_011532780.1:p.Asp1424=
|
|
XM_011534482.1:c.4059C>T
|
XP_011532784.1:p.Asp1353=
|
|
XM_011534483.1:c.3981C>T
|
XP_011532785.1:p.Asp1327=
|
|
XM_011534484.1:c.3582C>T
|
XP_011532786.1:p.Asp1194=
|
|
XR_941095.1:n.4327C>T
|
|
|
XM_011534478.3:c.4272C>T
|
XP_011532780.1:p.Asp1424=
|
|
XM_011534484.2:c.3582C>T
|
XP_011532786.1:p.Asp1194=
|
|
XM_017009263.1:c.*187C>T
|
XP_016864752.1:n.*187C>T
|
|
XM_017009268.1:c.3963C>T
|
XP_016864757.1:p.Asp1321=
|
|
XR_001742050.2:n.4531C>T
|
|
|
NM_182925.5:c.4041C>T
MANE Select
|
NP_891555.2:p.Asp1347=
|
|