ENST00000247933.9:c.886T>G
|
ENSP00000247933.4:p.Tyr296Asp
|
|
ENST00000514224.2:c.886T>G
MANE Select
|
ENSP00000425081.2:p.Tyr296Asp
|
|
ENST00000652070.1:n.942T>G
|
|
|
ENST00000247933.8:c.886T>G
|
ENSP00000247933.4:p.Tyr296Asp
|
|
ENST00000514224.1:c.490T>G
|
ENSP00000425081.1:p.Tyr164Asp
|
|
ENST00000514698.5:n.886T>G
|
|
|
NM_000203.4:c.886T>G
|
NP_000194.2:p.Tyr296Asp
|
|
NR_110313.1:n.974T>G
|
|
|
XM_006713882.2:c.490T>G
|
XP_006713945.1:p.Tyr164Asp
|
|
XM_011513459.1:c.845T>G
|
XP_011511761.1:p.Leu282Ter
|
|
XM_011513460.1:c.745T>G
|
XP_011511762.1:p.Tyr249Asp
|
|
XM_011513461.1:c.679T>G
|
XP_011511763.1:p.Tyr227Asp
|
|
XM_011513462.1:c.598T>G
|
XP_011511764.1:p.Tyr200Asp
|
|
XM_011513463.1:c.598T>G
|
XP_011511765.1:p.Tyr200Asp
|
|
XR_924947.1:n.955T>G
|
|
|
NM_000203.5:c.886T>G
MANE Select
|
NP_000194.2:p.Tyr296Asp
|
|
NM_001363576.1:c.490T>G
|
NP_001350505.1:p.Tyr164Asp
|
|
XM_011513461.2:c.679T>G
|
XP_011511763.1:p.Tyr227Asp
|
|
XM_017008163.1:c.-75T>G
|
XP_016863652.1:n.-75T>G
|
|