ENST00000547400.6:c.977-57T=
|
ENSP00000446724.2:n.977-57T=
|
|
ENST00000551576.6:c.1247-57T=
|
ENSP00000455848.2:n.1247-57T=
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ENST00000552678.2:c.1247-57T=
|
ENSP00000457394.2:n.1247-57T=
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|
ENST00000388922.9:c.1247-57T=
MANE Select
|
ENSP00000373574.4:n.1247-57T=
|
|
ENST00000388922.8:c.1247-57T=
|
ENSP00000373574.4:n.1247-57T=
|
|
ENST00000419526.6:c.725-57T=
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ENSP00000392492.2:n.725-57T=
|
|
ENST00000547632.1:n.522-57T=
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|
|
ENST00000550683.5:c.1289-57T=
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ENSP00000447884.1:n.1289-57T=
|
|
ENST00000552678.1:c.252-57T=
|
|
|
NM_000020.2:c.1247-57T= , LRG_543t1:c.1247-57T=
|
NP_000011.2:n.1247-57T=
|
|
NM_001077401.1:c.1247-57T=
|
NP_001070869.1:n.1247-57T=
|
|
XM_005269235.2:c.1247-57T=
|
XP_005269292.1:n.1247-57T=
|
|
XM_011539008.1:c.977-57T=
|
XP_011537310.1:n.977-57T=
|
|
XM_024449279.1:c.458-57T=
|
XP_024305047.1:n.458-57T=
|
|
NM_000020.3:c.1247-57T=
MANE Select
|
NP_000011.2:n.1247-57T=
|
|
NM_001077401.2:c.1247-57T=
|
NP_001070869.1:n.1247-57T=
|
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