ENST00000317961.9:c.3318G>T
MANE Select
|
ENSP00000322408.4:p.Met1106Ile
|
|
ENST00000317961.8:c.3318G>T
|
ENSP00000322408.4:p.Met1106Ile
|
|
ENST00000382806.6:c.3147G>T
|
ENSP00000372256.2:p.Met1049Ile
|
|
ENST00000415360.1:c.234G>T
|
ENSP00000389433.1:p.Met78Ile
|
|
ENST00000440077.5:c.3195G>T
|
ENSP00000398543.1:p.Met1065Ile
|
|
ENST00000469599.6:n.1916G>T
|
|
|
ENST00000492117.1:n.3210G>T
|
|
|
ENST00000541639.5:c.3411G>T
|
ENSP00000444293.1:p.Met1137Ile
|
|
NM_001146705.1:c.3411G>T
|
NP_001140177.1:p.Met1137Ile
|
|
NM_001146706.1:c.3147G>T
|
NP_001140178.1:p.Met1049Ile
|
|
NM_004653.4:c.3318G>T
|
NP_004644.2:p.Met1106Ile
|
|
XM_005262560.1:c.3183G>T
|
XP_005262617.1:p.Met1061Ile
|
|
XM_005262561.1:c.3087G>T
|
XP_005262618.1:p.Met1029Ile
|
|
XM_011531468.1:c.3240G>T
|
XP_011529770.1:p.Met1080Ile
|
|
XR_244571.2:n.3606G>T
|
|
|
XR_430568.2:n.3940G>T
|
|
|
XM_005262560.3:c.3183G>T
|
XP_005262617.1:p.Met1061Ile
|
|
XM_005262561.3:c.3087G>T
|
XP_005262618.1:p.Met1029Ile
|
|
XM_011531468.3:c.3240G>T
|
XP_011529770.1:p.Met1080Ile
|
|
XM_024452495.1:c.1308G>T
|
XP_024308263.1:p.Met436Ile
|
|
XM_024452496.1:c.1074G>T
|
XP_024308264.1:p.Met358Ile
|
|
XR_001756009.2:n.4056G>T
|
|
|
XR_001756010.2:n.4056G>T
|
|
|
XR_001756011.2:n.3921G>T
|
|
|
XR_001756012.2:n.4069G>T
|
|
|
XR_001756013.2:n.3387G>T
|
|
|
XR_002958832.1:n.3488G>T
|
|
|
XR_002958834.1:n.3712G>T
|
|
|
XR_002958835.1:n.3595G>T
|
|
|
XR_002958836.1:n.4278G>T
|
|
|
XR_002958837.1:n.4085G>T
|
|
|
XR_244571.4:n.3605G>T
|
|
|
XR_430568.4:n.3939G>T
|
|
|
NM_001146706.2:c.3147G>T
|
NP_001140178.1:p.Met1049Ile
|
|
NM_004653.5:c.3318G>T
MANE Select
|
NP_004644.2:p.Met1106Ile
|
|
NM_001146705.2:c.3411G>T
|
NP_001140177.1:p.Met1137Ile
|
|