ENST00000704289.1:c.*905C>A
|
ENSP00000515816.1:n.*905C>A
|
|
ENST00000315285.9:c.1245C>A
MANE Select
|
ENSP00000320885.3:p.Tyr415Ter
|
|
ENST00000621856.2:c.1242C>A
|
ENSP00000482496.2:p.Tyr414Ter
|
|
ENST00000642281.1:c.983-8084C>A
|
|
|
ENST00000642455.1:c.1146C>A
|
ENSP00000493827.1:p.Tyr382Ter
|
|
ENST00000642751.1:c.1019C>A
|
|
|
ENST00000642999.1:c.987C>A
|
ENSP00000496589.1:p.Tyr329Ter
|
|
ENST00000643327.1:c.404C>A
|
|
|
ENST00000643334.1:c.825C>A
|
|
|
ENST00000644408.1:c.1121C>A
|
|
|
ENST00000644954.1:c.891C>A
|
ENSP00000494312.1:p.Tyr297Ter
|
|
ENST00000645159.1:n.1982C>A
|
|
|
ENST00000645550.1:n.458C>A
|
|
|
ENST00000645671.1:c.695C>A
|
|
|
ENST00000645730.1:c.592C>A
|
|
|
ENST00000646082.1:c.891C>A
|
|
|
ENST00000646571.1:c.1149C>A
|
ENSP00000495015.1:p.Tyr383Ter
|
|
ENST00000647007.1:n.937C>A
|
|
|
ENST00000647133.1:c.745C>A
|
|
|
ENST00000315285.7:c.1245C>A
|
ENSP00000320885.3:p.Tyr415Ter
|
|
ENST00000345662.5:c.1149C>A
|
ENSP00000340817.1:p.Tyr383Ter
|
|
ENST00000615843.4:c.1245C>A
|
ENSP00000480893.1:p.Tyr415Ter
|
|
ENST00000621856.1:c.987C>A
|
ENSP00000482496.1:p.Tyr329Ter
|
|
NM_014946.3:c.1245C>A , LRG_714t1:c.1245C>A
|
NP_055761.2:p.Tyr415Ter
|
|
NM_199436.1:c.1149C>A
|
NP_955468.1:p.Tyr383Ter
|
|
XM_005264516.3:c.1242C>A
|
XP_005264573.1:p.Tyr414Ter
|
|
XM_011533067.1:c.1245C>A
|
XP_011531369.1:p.Tyr415Ter
|
|
NM_001363823.1:c.1242C>A
|
NP_001350752.1:p.Tyr414Ter
|
|
NM_001363875.1:c.1146C>A
|
NP_001350804.1:p.Tyr382Ter
|
|
XM_005264516.5:c.1242C>A
|
XP_005264573.1:p.Tyr414Ter
|
|
XM_011533067.2:c.1245C>A
|
XP_011531369.1:p.Tyr415Ter
|
|
XM_017004778.2:c.1149C>A
|
XP_016860267.1:p.Tyr383Ter
|
|
NM_001363823.2:c.1242C>A
|
NP_001350752.1:p.Tyr414Ter
|
|
NM_001363875.2:c.1146C>A
|
NP_001350804.1:p.Tyr382Ter
|
|
NM_001377959.1:c.1149C>A
|
NP_001364888.1:p.Tyr383Ter
|
|
NM_014946.4:c.1245C>A
MANE Select
|
NP_055761.2:p.Tyr415Ter
|
|
NM_199436.2:c.1149C>A
|
NP_955468.1:p.Tyr383Ter
|
|