ENST00000348974.5:c.1762A=
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ENSP00000330021.7:p.Thr588=
|
|
ENST00000394236.9:c.1762A=
MANE Select
|
ENSP00000377783.3:p.Thr588=
|
|
ENST00000407433.6:c.1717A=
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ENSP00000385794.2:p.Thr573=
|
|
ENST00000647936.1:c.1644+2089A=
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ENSP00000496822.1:n.1644+2089A=
|
|
ENST00000648381.1:n.1930A=
|
|
|
ENST00000648853.1:c.1720A=
|
ENSP00000497262.1:p.Thr574=
|
|
ENST00000649103.1:c.1861A=
|
ENSP00000497962.1:n.1861A=
|
|
ENST00000649585.1:c.705A=
|
ENSP00000498163.1:n.705A=
|
|
ENST00000650591.1:c.1858A=
|
ENSP00000497376.1:p.Thr620=
|
|
ENST00000394236.7:c.1762A=
|
ENSP00000377783.3:p.Thr588=
|
|
ENST00000407433.5:c.1369A=
|
ENSP00000385794.1:p.Thr457=
|
|
NM_000313.3:c.1762A= , LRG_572t1:c.1762A=
|
NP_000304.2:p.Thr588=
|
|
NM_001314077.1:c.1858A= , LRG_572t2:c.1858A=
|
NP_001301006.1:p.Thr620=
|
|
NM_000313.4:c.1762A=
MANE Select
|
NP_000304.2:p.Thr588=
|
|
NM_001314077.2:c.1858A=
|
NP_001301006.1:p.Thr620=
|
|