ENST00000394867.9:n.1782A=
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|
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ENST00000688751.1:n.479A=
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|
|
ENST00000689792.1:n.1247A=
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|
|
ENST00000262948.10:c.*140A=
MANE Select
|
ENSP00000262948.4:n.*140A=
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ENST00000262948.9:c.*140A=
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ENSP00000262948.3:n.*140A=
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ENST00000394867.8:c.*140A=
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ENSP00000378336.1:n.*140A=
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ENST00000597263.5:n.528A=
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ENST00000600584.5:n.2792A=
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|
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ENST00000601786.5:n.1644A=
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|
|
NM_030662.3:c.*140A= , LRG_750t1:c.*140A=
|
NP_109587.1:n.*140A=
|
|
XM_006722799.2:c.*140A=
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XP_006722862.1:n.*140A=
|
|
XM_011528133.1:c.*140A=
|
XP_011526435.1:n.*140A=
|
|
NM_030662.4:c.*140A=
MANE Select
|
NP_109587.1:n.*140A=
|
|