ENST00000237596.7:c.1139G>C
MANE Select
|
ENSP00000237596.2:p.Trp380Ser
|
|
ENST00000237596.6:c.1139G>C
|
ENSP00000237596.2:p.Trp380Ser
|
|
ENST00000506367.1:n.586G>C
|
|
|
ENST00000508588.5:c.-379G>C
|
ENSP00000427131.1:n.-379G>C
|
|
NM_000297.3:c.1139G>C
|
NP_000288.1:p.Trp380Ser
|
|
XM_011532028.1:c.1095-3365G>C
|
XP_011530330.1:n.1095-3365G>C
|
|
XM_011532029.1:c.419G>C
|
XP_011530331.1:p.Trp140Ser
|
|
XM_011532030.1:c.299G>C
|
XP_011530332.1:p.Trp100Ser
|
|
XR_244632.2:n.1234G>C
|
|
|
NR_156488.1:n.1226G>C
|
|
|
XM_011532028.2:c.1095-3365G>C
|
XP_011530330.1:n.1095-3365G>C
|
|
XM_011532030.2:c.299G>C
|
XP_011530332.1:p.Trp100Ser
|
|
NM_000297.4:c.1139G>C
MANE Select
|
NP_000288.1:p.Trp380Ser
|
|
NR_156488.2:n.1238G>C
|
|
|