ENST00000298854.7:c.1232T>C
MANE Select
|
ENSP00000298854.2:p.Phe411Ser
|
|
ENST00000298854.6:c.1232T>C
|
ENSP00000298854.2:p.Phe411Ser
|
|
ENST00000352508.7:c.1055T>C
|
ENSP00000298853.3:p.Phe352Ser
|
|
ENST00000524487.5:c.1073T>C
|
ENSP00000435551.2:p.Phe358Ser
|
|
ENST00000528356.1:n.187T>C
|
|
|
NM_005055.4:c.1232T>C
|
NP_005046.2:p.Phe411Ser
|
|
NM_032645.4:c.1055T>C
|
NP_116034.2:p.Phe352Ser
|
|
XM_005253042.2:c.1178T>C
|
XP_005253099.1:p.Phe393Ser
|
|
XM_005253043.2:c.1109T>C
|
XP_005253100.1:p.Phe370Ser
|
|
XM_011520252.1:c.1317T>C
|
XP_011518554.1:p.Leu439=
|
|
XM_011520253.1:c.1256T>C
|
XP_011518555.1:p.Phe419Ser
|
|
XM_005253042.3:c.1178T>C
|
XP_005253099.1:p.Phe393Ser
|
|
XM_005253043.3:c.1109T>C
|
XP_005253100.1:p.Phe370Ser
|
|
NM_005055.5:c.1232T>C
MANE Select
|
NP_005046.2:p.Phe411Ser
|
|
NM_032645.5:c.1055T>C
|
NP_116034.2:p.Phe352Ser
|
|