ENST00000394867.9:n.1850G=
|
|
|
ENST00000688751.1:n.547G=
|
|
|
ENST00000689792.1:n.1315G=
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|
|
ENST00000262948.10:c.*208G=
MANE Select
|
ENSP00000262948.4:n.*208G=
|
|
ENST00000262948.9:c.*208G=
|
ENSP00000262948.3:n.*208G=
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|
ENST00000394867.8:c.*208G=
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ENSP00000378336.1:n.*208G=
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|
ENST00000600584.5:n.2860G=
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|
|
ENST00000601786.5:n.1712G=
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|
|
NM_030662.3:c.*208G= , LRG_750t1:c.*208G=
|
NP_109587.1:n.*208G=
|
|
XM_006722799.2:c.*208G=
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XP_006722862.1:n.*208G=
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|
XM_011528133.1:c.*208G=
|
XP_011526435.1:n.*208G=
|
|
NM_030662.4:c.*208G=
MANE Select
|
NP_109587.1:n.*208G=
|
|