ENST00000394867.9:n.1203T>C
|
|
|
ENST00000687128.1:n.1203T>C
|
|
|
ENST00000688002.1:n.1058T>C
|
|
|
ENST00000689792.1:n.668T>C
|
|
|
ENST00000262948.10:c.764T>C
MANE Select
|
ENSP00000262948.4:p.Leu255Pro
|
|
ENST00000262948.9:c.764T>C
|
ENSP00000262948.3:p.Leu255Pro
|
|
ENST00000394867.8:c.473T>C
|
ENSP00000378336.1:p.Leu158Pro
|
|
ENST00000593364.5:n.711T>C
|
|
|
ENST00000595715.1:n.579T>C
|
|
|
ENST00000597263.5:n.169+1663T>C
|
|
|
ENST00000599021.1:c.29+1663T>C
|
|
|
ENST00000600584.5:n.1324T>C
|
|
|
ENST00000601786.5:n.1065T>C
|
|
|
NM_030662.3:c.764T>C , LRG_750t1:c.764T>C
|
NP_109587.1:p.Leu255Pro
|
|
XM_006722799.2:c.705+1663T>C
|
XP_006722862.1:n.705+1663T>C
|
|
XM_011528133.1:c.194T>C
|
XP_011526435.1:p.Leu65Pro
|
|
XM_017026989.1:c.764T>C
|
XP_016882478.1:p.Leu255Pro
|
|
XM_017026990.1:c.705+1663T>C
|
XP_016882479.1:n.705+1663T>C
|
|
NM_030662.4:c.764T>C
MANE Select
|
NP_109587.1:p.Leu255Pro
|
|