ENST00000348974.5:c.917T>A
|
ENSP00000330021.7:p.Phe306Tyr
|
|
ENST00000394236.9:c.917T>A
MANE Select
|
ENSP00000377783.3:p.Phe306Tyr
|
|
ENST00000407433.6:c.872T>A
|
ENSP00000385794.2:p.Phe291Tyr
|
|
ENST00000647936.1:c.917T>A
|
ENSP00000496822.1:p.Phe306Tyr
|
|
ENST00000648381.1:n.1085T>A
|
|
|
ENST00000648853.1:c.875T>A
|
ENSP00000497262.1:p.Phe292Tyr
|
|
ENST00000649103.1:c.1016T>A
|
ENSP00000497962.1:n.1016T>A
|
|
ENST00000650591.1:c.1013T>A
|
ENSP00000497376.1:p.Phe338Tyr
|
|
ENST00000394236.7:c.917T>A
|
ENSP00000377783.3:p.Phe306Tyr
|
|
ENST00000407433.5:c.524T>A
|
ENSP00000385794.1:p.Phe175Tyr
|
|
NM_000313.3:c.917T>A , LRG_572t1:c.917T>A
|
NP_000304.2:p.Phe306Tyr
|
|
NM_001314077.1:c.1013T>A , LRG_572t2:c.1013T>A
|
NP_001301006.1:p.Phe338Tyr
|
|
NM_000313.4:c.917T>A
MANE Select
|
NP_000304.2:p.Phe306Tyr
|
|
NM_001314077.2:c.1013T>A
|
NP_001301006.1:p.Phe338Tyr
|
|