ENST00000303941.4:c.1214A>C
MANE Select
|
ENSP00000306678.3:p.Asp405Ala
|
|
ENST00000303941.3:c.1214A>C
|
ENSP00000306678.3:p.Asp405Ala
|
|
NM_178510.1:c.1214A>C
|
NP_848605.1:p.Asp405Ala
|
|
XM_011542736.1:c.1247A>C
|
XP_011541038.1:p.Asp416Ala
|
|
XM_011542737.1:c.1217A>C
|
XP_011541039.1:p.Asp406Ala
|
|
XM_011542738.1:c.1025A>C
|
XP_011541040.1:p.Asp342Ala
|
|
XM_011542736.2:c.1247A>C
|
XP_011541038.1:p.Asp416Ala
|
|
XM_011542737.2:c.1217A>C
|
XP_011541039.1:p.Asp406Ala
|
|
XM_011542738.2:c.1025A>C
|
XP_011541040.1:p.Asp342Ala
|
|
XM_017017475.1:c.1244A>C
|
XP_016872964.1:p.Asp415Ala
|
|
NM_178510.2:c.1214A>C
MANE Select
|
NP_848605.1:p.Asp405Ala
|
|