ENST00000370263.9:c.800T=
MANE Select
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ENSP00000359285.4:p.Leu267=
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ENST00000370263.8:c.800T=
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ENSP00000359285.4:p.Leu267=
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|
ENST00000463705.5:n.1448T=
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ENST00000467563.3:n.870T=
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ENST00000498043.6:c.824T=
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|
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ENST00000615287.4:c.587T=
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ENSP00000483388.1:p.Leu196=
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|
ENST00000627000.1:c.*489T=
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ENSP00000486914.1:n.*489T=
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ENST00000630240.1:n.521T=
|
|
|
NM_000744.6:c.800T=
|
NP_000735.1:p.Leu267=
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NM_001256573.1:c.272T=
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NP_001243502.1:p.Leu91=
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NR_046317.1:n.1056T=
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|
|
XM_011528524.1:c.587T=
|
XP_011526826.1:p.Leu196=
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|
XM_017027625.2:c.272T=
|
XP_016883114.1:p.Leu91=
|
|
XM_024451822.1:c.272T=
|
XP_024307590.1:p.Leu91=
|
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NM_001256573.2:c.272T=
|
NP_001243502.1:p.Leu91=
|
|
NR_046317.2:n.1009T=
|
|
|
NM_000744.7:c.800T=
MANE Select
|
NP_000735.1:p.Leu267=
|
|