ENST00000470094.2:c.7872T=
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ENSP00000434898.2:p.Tyr2624=
|
|
ENST00000528762.2:c.7872T=
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ENSP00000433168.2:p.Tyr2624=
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ENST00000530893.7:c.7503T=
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ENSP00000499438.2:p.Tyr2501=
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ENST00000665585.2:c.7872T=
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ENSP00000499570.2:p.Tyr2624=
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ENST00000666593.2:c.7872T=
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ENSP00000499256.2:p.Tyr2624=
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|
ENST00000700202.2:c.7872T=
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ENSP00000514856.2:p.Tyr2624=
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ENST00000700202.1:c.339T=
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ENSP00000514856.1:p.Tyr113=
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|
ENST00000380152.8:c.7872T=
MANE Select
|
ENSP00000369497.3:p.Tyr2624=
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|
ENST00000544455.6:c.7872T=
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ENSP00000439902.1:p.Tyr2624=
|
|
ENST00000614259.2:c.7880T=
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ENSP00000506251.1:p.Ile2627=
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|
ENST00000665585.1:c.437T=
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|
|
ENST00000680887.1:c.7872T=
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ENSP00000505508.1:p.Tyr2624=
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|
ENST00000380152.7:c.7872T=
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ENSP00000369497.3:p.Tyr2624=
|
|
ENST00000544455.5:c.7872T=
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ENSP00000439902.1:p.Tyr2624=
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|
ENST00000614259.1:n.7880T=
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|
|
NM_000059.3:c.7872T= , LRG_293t1:c.7872T=
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NP_000050.2:p.Tyr2624=
|
|
XM_011535203.1:c.7872T=
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XP_011533505.1:p.Tyr2624=
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|
XM_011535204.1:c.7776T=
|
XP_011533506.1:p.Tyr2592=
|
|
XM_011535205.1:c.7872T=
|
XP_011533507.1:p.Tyr2624=
|
|
NM_000059.4:c.7872T=
MANE Select
|
NP_000050.3:p.Tyr2624=
|
|