|
ENST00000704289.1:c.*163G>C
|
ENSP00000515816.1:n.*163G>C
|
|
|
ENST00000315285.9:c.503G>C
MANE Select
|
ENSP00000320885.3:p.Gly168Ala
|
|
|
ENST00000621856.2:c.500G>C
|
ENSP00000482496.2:p.Gly167Ala
|
|
|
ENST00000642281.1:c.387G>C
|
|
|
|
ENST00000642455.1:c.500G>C
|
ENSP00000493827.1:p.Gly167Ala
|
|
|
ENST00000642751.1:c.373G>C
|
|
|
|
ENST00000642999.1:c.245G>C
|
ENSP00000496589.1:p.Gly82Ala
|
|
|
ENST00000643334.1:c.88G>C
|
|
|
|
ENST00000644408.1:c.379G>C
|
|
|
|
ENST00000644954.1:c.245G>C
|
ENSP00000494312.1:p.Gly82Ala
|
|
|
ENST00000645400.1:c.459G>C
|
ENSP00000496306.1:n.459G>C
|
|
|
ENST00000645671.1:c.37-9274G>C
|
|
|
|
ENST00000646082.1:c.337G>C
|
|
|
|
ENST00000646571.1:c.503G>C
|
ENSP00000495015.1:p.Gly168Ala
|
|
|
ENST00000647007.1:n.200G>C
|
|
|
|
ENST00000647133.1:c.78G>C
|
|
|
|
ENST00000315285.7:c.503G>C
|
ENSP00000320885.3:p.Gly168Ala
|
|
|
ENST00000345662.5:c.503G>C
|
ENSP00000340817.1:p.Gly168Ala
|
|
|
ENST00000615843.4:c.503G>C
|
ENSP00000480893.1:p.Gly168Ala
|
|
|
ENST00000621856.1:c.245G>C
|
ENSP00000482496.1:p.Gly82Ala
|
|
|
NM_014946.3:c.503G>C , LRG_714t1:c.503G>C
|
NP_055761.2:p.Gly168Ala
|
|
|
NM_199436.1:c.503G>C
|
NP_955468.1:p.Gly168Ala
|
|
|
XM_005264516.3:c.500G>C
|
XP_005264573.1:p.Gly167Ala
|
|
|
XM_011533067.1:c.503G>C
|
XP_011531369.1:p.Gly168Ala
|
|
|
NM_001363823.1:c.500G>C
|
NP_001350752.1:p.Gly167Ala
|
|
|
NM_001363875.1:c.500G>C
|
NP_001350804.1:p.Gly167Ala
|
|
|
XM_005264516.5:c.500G>C
|
XP_005264573.1:p.Gly167Ala
|
|
|
XM_011533067.2:c.503G>C
|
XP_011531369.1:p.Gly168Ala
|
|
|
XM_017004778.2:c.503G>C
|
XP_016860267.1:p.Gly168Ala
|
|
|
NM_001363823.2:c.500G>C
|
NP_001350752.1:p.Gly167Ala
|
|
|
NM_001363875.2:c.500G>C
|
NP_001350804.1:p.Gly167Ala
|
|
|
NM_001377959.1:c.503G>C
|
NP_001364888.1:p.Gly168Ala
|
|
|
NM_014946.4:c.503G>C
MANE Select
|
NP_055761.2:p.Gly168Ala
|
|
|
NM_199436.2:c.503G>C
|
NP_955468.1:p.Gly168Ala
|
|
