ENST00000394867.9:n.1426A=
|
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ENST00000688002.1:n.3138A=
|
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ENST00000688751.1:n.123A=
|
|
|
ENST00000689792.1:n.891A=
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|
|
ENST00000262948.10:c.987A=
MANE Select
|
ENSP00000262948.4:p.Pro329=
|
|
ENST00000262948.9:c.987A=
|
ENSP00000262948.3:p.Pro329=
|
|
ENST00000394867.8:c.696A=
|
ENSP00000378336.1:p.Pro232=
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|
ENST00000595715.1:n.802A=
|
|
|
ENST00000597263.5:n.172A=
|
|
|
ENST00000599021.1:c.97A=
|
|
|
ENST00000600584.5:n.1547A=
|
|
|
ENST00000601786.5:n.1288A=
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|
|
NM_030662.3:c.987A= , LRG_750t1:c.987A=
|
NP_109587.1:p.Pro329=
|
|
XM_006722799.2:c.708A=
|
XP_006722862.1:p.Pro236=
|
|
XM_011528133.1:c.417A=
|
XP_011526435.1:p.Pro139=
|
|
XM_017026989.1:c.987A=
|
XP_016882478.1:p.Pro329=
|
|
XM_017026990.1:c.708A=
|
XP_016882479.1:p.Pro236=
|
|
NM_030662.4:c.987A=
MANE Select
|
NP_109587.1:p.Pro329=
|
|