ENST00000317961.9:c.3289T>A
MANE Select
|
ENSP00000322408.4:p.Ser1097Thr
|
|
ENST00000317961.8:c.3289T>A
|
ENSP00000322408.4:p.Ser1097Thr
|
|
ENST00000382806.6:c.3118T>A
|
ENSP00000372256.2:p.Ser1040Thr
|
|
ENST00000415360.1:c.205T>A
|
ENSP00000389433.1:p.Ser69Thr
|
|
ENST00000440077.5:c.3166T>A
|
ENSP00000398543.1:p.Ser1056Thr
|
|
ENST00000469599.6:n.1887T>A
|
|
|
ENST00000492117.1:n.3181T>A
|
|
|
ENST00000541639.5:c.3382T>A
|
ENSP00000444293.1:p.Ser1128Thr
|
|
NM_001146705.1:c.3382T>A
|
NP_001140177.1:p.Ser1128Thr
|
|
NM_001146706.1:c.3118T>A
|
NP_001140178.1:p.Ser1040Thr
|
|
NM_004653.4:c.3289T>A
|
NP_004644.2:p.Ser1097Thr
|
|
XM_005262560.1:c.3154T>A
|
XP_005262617.1:p.Ser1052Thr
|
|
XM_005262561.1:c.3058T>A
|
XP_005262618.1:p.Ser1020Thr
|
|
XM_011531468.1:c.3211T>A
|
XP_011529770.1:p.Ser1071Thr
|
|
XR_244571.2:n.3577T>A
|
|
|
XR_430568.2:n.3911T>A
|
|
|
XM_005262560.3:c.3154T>A
|
XP_005262617.1:p.Ser1052Thr
|
|
XM_005262561.3:c.3058T>A
|
XP_005262618.1:p.Ser1020Thr
|
|
XM_011531468.3:c.3211T>A
|
XP_011529770.1:p.Ser1071Thr
|
|
XM_024452495.1:c.1279T>A
|
XP_024308263.1:p.Ser427Thr
|
|
XM_024452496.1:c.1045T>A
|
XP_024308264.1:p.Ser349Thr
|
|
XR_001756009.2:n.4027T>A
|
|
|
XR_001756010.2:n.4027T>A
|
|
|
XR_001756011.2:n.3892T>A
|
|
|
XR_001756012.2:n.4040T>A
|
|
|
XR_001756013.2:n.3358T>A
|
|
|
XR_002958832.1:n.3459T>A
|
|
|
XR_002958834.1:n.3683T>A
|
|
|
XR_002958835.1:n.3566T>A
|
|
|
XR_002958836.1:n.4249T>A
|
|
|
XR_002958837.1:n.4056T>A
|
|
|
XR_244571.4:n.3576T>A
|
|
|
XR_430568.4:n.3910T>A
|
|
|
NM_001146706.2:c.3118T>A
|
NP_001140178.1:p.Ser1040Thr
|
|
NM_004653.5:c.3289T>A
MANE Select
|
NP_004644.2:p.Ser1097Thr
|
|
NM_001146705.2:c.3382T>A
|
NP_001140177.1:p.Ser1128Thr
|
|