ENST00000303941.4:c.1963G>A
MANE Select
|
ENSP00000306678.3:p.Ala655Thr
|
|
ENST00000303941.3:c.1963G>A
|
ENSP00000306678.3:p.Ala655Thr
|
|
NM_178510.1:c.1963G>A
|
NP_848605.1:p.Ala655Thr
|
|
XM_011542736.1:c.1996G>A
|
XP_011541038.1:p.Ala666Thr
|
|
XM_011542737.1:c.1966G>A
|
XP_011541039.1:p.Ala656Thr
|
|
XM_011542738.1:c.1774G>A
|
XP_011541040.1:p.Ala592Thr
|
|
XM_011542736.2:c.1996G>A
|
XP_011541038.1:p.Ala666Thr
|
|
XM_011542737.2:c.1966G>A
|
XP_011541039.1:p.Ala656Thr
|
|
XM_011542738.2:c.1774G>A
|
XP_011541040.1:p.Ala592Thr
|
|
XM_017017475.1:c.1993G>A
|
XP_016872964.1:p.Ala665Thr
|
|
NM_178510.2:c.1963G>A
MANE Select
|
NP_848605.1:p.Ala655Thr
|
|