|
ENST00000704289.1:c.*932G>T
|
ENSP00000515816.1:n.*932G>T
|
|
|
ENST00000315285.9:c.1272G>T
MANE Select
|
ENSP00000320885.3:p.Arg424Ser
|
|
|
ENST00000621856.2:c.1269G>T
|
ENSP00000482496.2:p.Arg423Ser
|
|
|
ENST00000642281.1:c.1009G>T
|
|
|
|
ENST00000642455.1:c.1173G>T
|
ENSP00000493827.1:p.Arg391Ser
|
|
|
ENST00000642751.1:c.1046G>T
|
|
|
|
ENST00000642999.1:c.1014G>T
|
ENSP00000496589.1:p.Arg338Ser
|
|
|
ENST00000643327.1:c.431G>T
|
|
|
|
ENST00000643334.1:c.852G>T
|
|
|
|
ENST00000644408.1:c.1148G>T
|
|
|
|
ENST00000644954.1:c.918G>T
|
ENSP00000494312.1:p.Arg306Ser
|
|
|
ENST00000645159.1:n.2009G>T
|
|
|
|
ENST00000645671.1:c.722G>T
|
|
|
|
ENST00000645730.1:c.593-520G>T
|
|
|
|
ENST00000646082.1:c.918G>T
|
|
|
|
ENST00000646571.1:c.1176G>T
|
ENSP00000495015.1:p.Arg392Ser
|
|
|
ENST00000647007.1:n.964G>T
|
|
|
|
ENST00000647133.1:c.772G>T
|
|
|
|
ENST00000315285.7:c.1272G>T
|
ENSP00000320885.3:p.Arg424Ser
|
|
|
ENST00000345662.5:c.1176G>T
|
ENSP00000340817.1:p.Arg392Ser
|
|
|
ENST00000615843.4:c.1272G>T
|
ENSP00000480893.1:p.Arg424Ser
|
|
|
ENST00000621856.1:c.1014G>T
|
ENSP00000482496.1:p.Arg338Ser
|
|
|
NM_014946.3:c.1272G>T , LRG_714t1:c.1272G>T
|
NP_055761.2:p.Arg424Ser
|
|
|
NM_199436.1:c.1176G>T
|
NP_955468.1:p.Arg392Ser
|
|
|
XM_005264516.3:c.1269G>T
|
XP_005264573.1:p.Arg423Ser
|
|
|
XM_011533067.1:c.1272G>T
|
XP_011531369.1:p.Arg424Ser
|
|
|
NM_001363823.1:c.1269G>T
|
NP_001350752.1:p.Arg423Ser
|
|
|
NM_001363875.1:c.1173G>T
|
NP_001350804.1:p.Arg391Ser
|
|
|
XM_005264516.5:c.1269G>T
|
XP_005264573.1:p.Arg423Ser
|
|
|
XM_011533067.2:c.1272G>T
|
XP_011531369.1:p.Arg424Ser
|
|
|
XM_017004778.2:c.1176G>T
|
XP_016860267.1:p.Arg392Ser
|
|
|
NM_001363823.2:c.1269G>T
|
NP_001350752.1:p.Arg423Ser
|
|
|
NM_001363875.2:c.1173G>T
|
NP_001350804.1:p.Arg391Ser
|
|
|
NM_001377959.1:c.1176G>T
|
NP_001364888.1:p.Arg392Ser
|
|
|
NM_014946.4:c.1272G>T
MANE Select
|
NP_055761.2:p.Arg424Ser
|
|
|
NM_199436.2:c.1176G>T
|
NP_955468.1:p.Arg392Ser
|
|
