ENST00000370263.9:c.602T=
MANE Select
|
ENSP00000359285.4:p.Leu201=
|
|
ENST00000370263.8:c.602T=
|
ENSP00000359285.4:p.Leu201=
|
|
ENST00000463705.5:n.1250T=
|
|
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ENST00000467563.3:n.672T=
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|
|
ENST00000498043.6:c.626T=
|
|
|
ENST00000615287.4:c.389T=
|
ENSP00000483388.1:p.Leu130=
|
|
ENST00000627000.1:c.*291T=
|
ENSP00000486914.1:n.*291T=
|
|
ENST00000630240.1:n.323T=
|
|
|
NM_000744.6:c.602T=
|
NP_000735.1:p.Leu201=
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|
NM_001256573.1:c.74T=
|
NP_001243502.1:p.Leu25=
|
|
NR_046317.1:n.858T=
|
|
|
XM_011528524.1:c.389T=
|
XP_011526826.1:p.Leu130=
|
|
XM_017027625.2:c.74T=
|
XP_016883114.1:p.Leu25=
|
|
XM_024451822.1:c.74T=
|
XP_024307590.1:p.Leu25=
|
|
NM_001256573.2:c.74T=
|
NP_001243502.1:p.Leu25=
|
|
NR_046317.2:n.811T=
|
|
|
NM_000744.7:c.602T=
MANE Select
|
NP_000735.1:p.Leu201=
|
|