ENST00000317961.9:c.3705G>C
MANE Select
|
ENSP00000322408.4:p.Met1235Ile
|
|
ENST00000317961.8:c.3705G>C
|
ENSP00000322408.4:p.Met1235Ile
|
|
ENST00000382806.6:c.3534G>C
|
ENSP00000372256.2:p.Met1178Ile
|
|
ENST00000415360.1:c.621G>C
|
ENSP00000389433.1:p.Met207Ile
|
|
ENST00000440077.5:c.3582G>C
|
ENSP00000398543.1:p.Met1194Ile
|
|
ENST00000469599.6:n.2303G>C
|
|
|
ENST00000492117.1:n.3597G>C
|
|
|
ENST00000541639.5:c.3798G>C
|
ENSP00000444293.1:p.Met1266Ile
|
|
NM_001146705.1:c.3798G>C
|
NP_001140177.1:p.Met1266Ile
|
|
NM_001146706.1:c.3534G>C
|
NP_001140178.1:p.Met1178Ile
|
|
NM_004653.4:c.3705G>C
|
NP_004644.2:p.Met1235Ile
|
|
XM_005262560.1:c.3570G>C
|
XP_005262617.1:p.Met1190Ile
|
|
XM_005262561.1:c.3474G>C
|
XP_005262618.1:p.Met1158Ile
|
|
XM_011531468.1:c.3627G>C
|
XP_011529770.1:p.Met1209Ile
|
|
XR_244571.2:n.3993G>C
|
|
|
XR_430568.2:n.4327G>C
|
|
|
XM_005262560.3:c.3570G>C
|
XP_005262617.1:p.Met1190Ile
|
|
XM_005262561.3:c.3474G>C
|
XP_005262618.1:p.Met1158Ile
|
|
XM_011531468.3:c.3627G>C
|
XP_011529770.1:p.Met1209Ile
|
|
XM_024452495.1:c.1695G>C
|
XP_024308263.1:p.Met565Ile
|
|
XM_024452496.1:c.1461G>C
|
XP_024308264.1:p.Met487Ile
|
|
XR_001756009.2:n.4443G>C
|
|
|
XR_001756010.2:n.4443G>C
|
|
|
XR_001756011.2:n.4308G>C
|
|
|
XR_001756012.2:n.4456G>C
|
|
|
XR_001756013.2:n.3774G>C
|
|
|
XR_002958832.1:n.3875G>C
|
|
|
XR_002958834.1:n.4099G>C
|
|
|
XR_002958835.1:n.3982G>C
|
|
|
XR_002958836.1:n.4665G>C
|
|
|
XR_002958837.1:n.4472G>C
|
|
|
XR_244571.4:n.3992G>C
|
|
|
XR_430568.4:n.4326G>C
|
|
|
NM_001146706.2:c.3534G>C
|
NP_001140178.1:p.Met1178Ile
|
|
NM_004653.5:c.3705G>C
MANE Select
|
NP_004644.2:p.Met1235Ile
|
|
NM_001146705.2:c.3798G>C
|
NP_001140177.1:p.Met1266Ile
|
|