ENST00000394867.9:n.1575T>C
|
|
|
ENST00000688002.1:n.3287T>C
|
|
|
ENST00000688751.1:n.272T>C
|
|
|
ENST00000689792.1:n.1040T>C
|
|
|
ENST00000262948.10:c.1136T>C
MANE Select
|
ENSP00000262948.4:p.Phe379Ser
|
|
ENST00000262948.9:c.1136T>C
|
ENSP00000262948.3:p.Phe379Ser
|
|
ENST00000394867.8:c.845T>C
|
ENSP00000378336.1:p.Phe282Ser
|
|
ENST00000597263.5:n.321T>C
|
|
|
ENST00000599021.1:c.246T>C
|
|
|
ENST00000600584.5:n.2585T>C
|
|
|
ENST00000601786.5:n.1437T>C
|
|
|
NM_030662.3:c.1136T>C , LRG_750t1:c.1136T>C
|
NP_109587.1:p.Phe379Ser
|
|
XM_006722799.2:c.857T>C
|
XP_006722862.1:p.Phe286Ser
|
|
XM_011528133.1:c.566T>C
|
XP_011526435.1:p.Phe189Ser
|
|
NM_030662.4:c.1136T>C
MANE Select
|
NP_109587.1:p.Phe379Ser
|
|