ENST00000394867.9:n.1580G=
|
|
|
ENST00000688002.1:n.3292G=
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|
|
ENST00000688751.1:n.277G=
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|
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ENST00000689792.1:n.1045G=
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|
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ENST00000262948.10:c.1141G=
MANE Select
|
ENSP00000262948.4:p.Gly381=
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|
ENST00000262948.9:c.1141G=
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ENSP00000262948.3:p.Gly381=
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|
ENST00000394867.8:c.850G=
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ENSP00000378336.1:p.Gly284=
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|
ENST00000597263.5:n.326G=
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|
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ENST00000599021.1:c.251G=
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|
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ENST00000600584.5:n.2590G=
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|
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ENST00000601786.5:n.1442G=
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|
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NM_030662.3:c.1141G= , LRG_750t1:c.1141G=
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NP_109587.1:p.Gly381=
|
|
XM_006722799.2:c.862G=
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XP_006722862.1:p.Gly288=
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XM_011528133.1:c.571G=
|
XP_011526435.1:p.Gly191=
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|
NM_030662.4:c.1141G=
MANE Select
|
NP_109587.1:p.Gly381=
|
|