ENST00000470094.2:c.9137T=
|
ENSP00000434898.2:p.Phe3046=
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|
ENST00000528762.2:c.*504T=
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ENSP00000433168.2:n.*504T=
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|
ENST00000530893.7:c.8768T=
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ENSP00000499438.2:p.Phe2923=
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|
ENST00000665585.2:c.*699T=
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ENSP00000499570.2:n.*699T=
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ENST00000666593.2:c.9137T=
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ENSP00000499256.2:p.Phe3046=
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|
ENST00000700202.2:c.9086T=
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ENSP00000514856.2:p.Phe3029=
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|
ENST00000700202.1:c.1553T=
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ENSP00000514856.1:p.Phe518=
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|
ENST00000700203.1:n.1264T=
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|
|
ENST00000380152.8:c.9137T=
MANE Select
|
ENSP00000369497.3:p.Phe3046=
|
|
ENST00000544455.6:c.9137T=
|
ENSP00000439902.1:p.Phe3046=
|
|
ENST00000614259.2:c.9145T=
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ENSP00000506251.1:n.9145T=
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|
ENST00000665585.1:c.2015T=
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|
|
ENST00000666593.1:c.20T=
|
ENSP00000499256.1:p.Phe7=
|
|
ENST00000680887.1:c.9137T=
|
ENSP00000505508.1:p.Phe3046=
|
|
ENST00000380152.7:c.9137T=
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ENSP00000369497.3:p.Phe3046=
|
|
ENST00000470094.1:c.94T=
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|
|
ENST00000544455.5:c.9137T=
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ENSP00000439902.1:p.Phe3046=
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|
NM_000059.3:c.9137T= , LRG_293t1:c.9137T=
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NP_000050.2:p.Phe3046=
|
|
XM_011535203.1:c.9137T=
|
XP_011533505.1:p.Phe3046=
|
|
XM_011535204.1:c.9041T=
|
XP_011533506.1:p.Phe3014=
|
|
NM_000059.4:c.9137T=
MANE Select
|
NP_000050.3:p.Phe3046=
|
|