ENST00000303941.4:c.2059G>T
MANE Select
|
ENSP00000306678.3:p.Ala687Ser
|
|
ENST00000303941.3:c.2059G>T
|
ENSP00000306678.3:p.Ala687Ser
|
|
NM_178510.1:c.2059G>T
|
NP_848605.1:p.Ala687Ser
|
|
XM_011542736.1:c.2092G>T
|
XP_011541038.1:p.Ala698Ser
|
|
XM_011542737.1:c.2062G>T
|
XP_011541039.1:p.Ala688Ser
|
|
XM_011542738.1:c.1870G>T
|
XP_011541040.1:p.Ala624Ser
|
|
XM_011542736.2:c.2092G>T
|
XP_011541038.1:p.Ala698Ser
|
|
XM_011542737.2:c.2062G>T
|
XP_011541039.1:p.Ala688Ser
|
|
XM_011542738.2:c.1870G>T
|
XP_011541040.1:p.Ala624Ser
|
|
XM_017017475.1:c.2089G>T
|
XP_016872964.1:p.Ala697Ser
|
|
NM_178510.2:c.2059G>T
MANE Select
|
NP_848605.1:p.Ala687Ser
|
|