ENST00000272321.12:c.1945A>G
MANE Select
|
ENSP00000272321.7:p.Met649Val
|
|
ENST00000272321.11:c.1945A>G
|
ENSP00000272321.7:p.Met649Val
|
|
ENST00000398544.7:c.1468A>G
|
ENSP00000381552.3:p.Met490Val
|
|
ENST00000409120.5:c.1369A>G
|
ENSP00000386769.1:p.Met457Val
|
|
ENST00000409199.5:c.1369A>G
|
ENSP00000386592.1:p.Met457Val
|
|
ENST00000409354.6:c.1203A>G
|
ENSP00000386795.2:p.Ile401Met
|
|
NM_001042692.2:c.1468A>G
|
NP_001036157.1:p.Met490Val
|
|
NM_015910.5:c.1945A>G
|
NP_056994.3:p.Met649Val
|
|
NR_122106.1:n.1588A>G
|
|
|
XM_005264348.2:c.1945A>G
|
XP_005264405.1:p.Met649Val
|
|
XM_011532881.1:c.1873A>G
|
XP_011531183.1:p.Met625Val
|
|
XM_011532882.1:c.1846A>G
|
XP_011531184.1:p.Met616Val
|
|
XM_011532883.1:c.1945A>G
|
XP_011531185.1:p.Met649Val
|
|
XR_244934.1:n.2188A>G
|
|
|
XR_244935.1:n.2089A>G
|
|
|
XR_939686.1:n.2426A>G
|
|
|
NM_001042692.3:c.1468A>G
|
NP_001036157.1:p.Met490Val
|
|
NM_001354044.1:c.1873A>G
|
NP_001340973.1:p.Met625Val
|
|
NM_015910.6:c.1945A>G
|
NP_056994.3:p.Met649Val
|
|
NR_122106.2:n.1588A>G
|
|
|
NR_148704.1:n.2721A>G
|
|
|
NR_148705.1:n.2370A>G
|
|
|
XM_005264348.4:c.1945A>G
|
XP_005264405.1:p.Met649Val
|
|
XM_011532881.3:c.1873A>G
|
XP_011531183.1:p.Met625Val
|
|
XR_001738759.2:n.2304A>G
|
|
|
XR_001738760.2:n.2402A>G
|
|
|
XR_002959303.1:n.2641A>G
|
|
|
XR_244934.3:n.2403A>G
|
|
|
NM_015910.7:c.1945A>G
MANE Select
|
NP_056994.3:p.Met649Val
|
|
NM_001354044.2:c.1873A>G
|
NP_001340973.1:p.Met625Val
|
|
NR_148704.2:n.2399A>G
|
|
|
NR_148705.2:n.2048A>G
|
|
|