ENST00000303941.4:c.1346A>C
MANE Select
|
ENSP00000306678.3:p.Asp449Ala
|
|
ENST00000303941.3:c.1346A>C
|
ENSP00000306678.3:p.Asp449Ala
|
|
NM_178510.1:c.1346A>C
|
NP_848605.1:p.Asp449Ala
|
|
XM_011542736.1:c.1379A>C
|
XP_011541038.1:p.Asp460Ala
|
|
XM_011542737.1:c.1349A>C
|
XP_011541039.1:p.Asp450Ala
|
|
XM_011542738.1:c.1157A>C
|
XP_011541040.1:p.Asp386Ala
|
|
XM_011542736.2:c.1379A>C
|
XP_011541038.1:p.Asp460Ala
|
|
XM_011542737.2:c.1349A>C
|
XP_011541039.1:p.Asp450Ala
|
|
XM_011542738.2:c.1157A>C
|
XP_011541040.1:p.Asp386Ala
|
|
XM_017017475.1:c.1376A>C
|
XP_016872964.1:p.Asp459Ala
|
|
NM_178510.2:c.1346A>C
MANE Select
|
NP_848605.1:p.Asp449Ala
|
|