ENST00000394867.9:n.1553T=
|
|
|
ENST00000688002.1:n.3265T=
|
|
|
ENST00000688751.1:n.250T=
|
|
|
ENST00000689792.1:n.1018T=
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|
|
ENST00000262948.10:c.1114T=
MANE Select
|
ENSP00000262948.4:p.Ser372=
|
|
ENST00000262948.9:c.1114T=
|
ENSP00000262948.3:p.Ser372=
|
|
ENST00000394867.8:c.823T=
|
ENSP00000378336.1:p.Ser275=
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|
ENST00000597263.5:n.299T=
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|
|
ENST00000599021.1:c.224T=
|
|
|
ENST00000600584.5:n.2563T=
|
|
|
ENST00000601786.5:n.1415T=
|
|
|
NM_030662.3:c.1114T= , LRG_750t1:c.1114T=
|
NP_109587.1:p.Ser372=
|
|
XM_006722799.2:c.835T=
|
XP_006722862.1:p.Ser279=
|
|
XM_011528133.1:c.544T=
|
XP_011526435.1:p.Ser182=
|
|
NM_030662.4:c.1114T=
MANE Select
|
NP_109587.1:p.Ser372=
|
|