ENST00000394867.9:n.1224T>C
|
|
|
ENST00000687128.1:n.1224T>C
|
|
|
ENST00000688002.1:n.1079T>C
|
|
|
ENST00000689792.1:n.689T>C
|
|
|
ENST00000262948.10:c.785T>C
MANE Select
|
ENSP00000262948.4:p.Val262Ala
|
|
ENST00000262948.9:c.785T>C
|
ENSP00000262948.3:p.Val262Ala
|
|
ENST00000394867.8:c.494T>C
|
ENSP00000378336.1:p.Val165Ala
|
|
ENST00000593364.5:n.732T>C
|
|
|
ENST00000595715.1:n.600T>C
|
|
|
ENST00000597263.5:n.169+1684T>C
|
|
|
ENST00000599021.1:c.29+1684T>C
|
|
|
ENST00000600584.5:n.1345T>C
|
|
|
ENST00000601786.5:n.1086T>C
|
|
|
NM_030662.3:c.785T>C , LRG_750t1:c.785T>C
|
NP_109587.1:p.Val262Ala
|
|
XM_006722799.2:c.705+1684T>C
|
XP_006722862.1:n.705+1684T>C
|
|
XM_011528133.1:c.215T>C
|
XP_011526435.1:p.Val72Ala
|
|
XM_017026989.1:c.785T>C
|
XP_016882478.1:p.Val262Ala
|
|
XM_017026990.1:c.705+1684T>C
|
XP_016882479.1:n.705+1684T>C
|
|
NM_030662.4:c.785T>C
MANE Select
|
NP_109587.1:p.Val262Ala
|
|