ENST00000697124.1:n.898G>T
|
|
|
ENST00000219596.6:c.1777G>T
MANE Select
|
ENSP00000219596.1:p.Ala593Ser
|
|
ENST00000219596.5:c.1777G>T
|
ENSP00000219596.1:p.Ala593Ser
|
|
ENST00000339854.8:c.1237G>T
|
ENSP00000339639.4:p.Ala413Ser
|
|
ENST00000536379.5:c.1144G>T
|
ENSP00000445079.1:p.Ala382Ser
|
|
ENST00000536980.5:c.*53G>T
|
ENSP00000444178.1:n.*53G>T
|
|
ENST00000537682.5:c.*53G>T
|
ENSP00000438611.1:n.*53G>T
|
|
ENST00000538326.5:c.*402G>T
|
ENSP00000437486.1:n.*402G>T
|
|
ENST00000539145.5:c.698G>T
|
ENSP00000444471.1:n.698G>T
|
|
ENST00000541159.5:c.1319G>T
|
ENSP00000438711.1:p.Arg440Leu
|
|
ENST00000542898.5:c.*53G>T
|
ENSP00000444615.1:n.*53G>T
|
|
ENST00000570511.5:c.1182G>T
|
ENSP00000458312.1:n.1182G>T
|
|
ENST00000572244.5:c.467G>T
|
ENSP00000461186.1:n.467G>T
|
|
ENST00000574583.5:c.549G>T
|
ENSP00000460269.1:n.549G>T
|
|
ENST00000576315.5:c.582G>T
|
ENSP00000460551.1:n.582G>T
|
|
ENST00000621655.1:c.1314G>T
|
ENSP00000481436.1:n.1314G>T
|
|
NM_000243.2:c.1777G>T , LRG_190t1:c.1777G>T
|
NP_000234.1:p.Ala593Ser
|
|
NM_001198536.1:c.1319G>T
|
NP_001185465.1:p.Arg440Leu
|
|
XM_017023236.2:c.1774G>T
|
XP_016878725.1:p.Ala592Ser
|
|
XR_001751903.1:n.2084G>T
|
|
|
NM_000243.3:c.1777G>T
MANE Select
|
NP_000234.1:p.Ala593Ser
|
|
NM_001198536.2:c.1319G>T
|
NP_001185465.2:p.Arg440Leu
|
|