ENST00000303941.4:c.1938G>T
MANE Select
|
ENSP00000306678.3:p.Leu646=
|
|
ENST00000303941.3:c.1938G>T
|
ENSP00000306678.3:p.Leu646=
|
|
NM_178510.1:c.1938G>T
|
NP_848605.1:p.Leu646=
|
|
XM_011542736.1:c.1971G>T
|
XP_011541038.1:p.Leu657=
|
|
XM_011542737.1:c.1941G>T
|
XP_011541039.1:p.Leu647=
|
|
XM_011542738.1:c.1749G>T
|
XP_011541040.1:p.Leu583=
|
|
XM_011542736.2:c.1971G>T
|
XP_011541038.1:p.Leu657=
|
|
XM_011542737.2:c.1941G>T
|
XP_011541039.1:p.Leu647=
|
|
XM_011542738.2:c.1749G>T
|
XP_011541040.1:p.Leu583=
|
|
XM_017017475.1:c.1968G>T
|
XP_016872964.1:p.Leu656=
|
|
NM_178510.2:c.1938G>T
MANE Select
|
NP_848605.1:p.Leu646=
|
|