ENST00000407991.3:c.1138A>G
MANE Select
|
ENSP00000385026.1:p.Met380Val
|
|
ENST00000240132.7:c.1093A>G
|
ENSP00000240132.2:p.Met365Val
|
|
ENST00000407991.2:c.1138A>G
|
ENSP00000385026.1:p.Met380Val
|
|
ENST00000520600.1:n.290-1551A>G
|
|
|
ENST00000520933.7:c.1072A>G
|
ENSP00000429616.2:p.Met358Val
|
|
ENST00000523695.5:c.*540A>G
|
ENSP00000430612.1:n.*540A>G
|
|
NM_000742.3:c.1138A>G
|
NP_000733.2:p.Met380Val
|
|
NM_001282455.1:c.1093A>G
|
NP_001269384.1:p.Met365Val
|
|
XM_005273397.1:c.661A>G
|
XP_005273454.1:p.Met221Val
|
|
XM_006716282.1:c.1138A>G
|
XP_006716345.1:p.Met380Val
|
|
XM_011544388.1:c.1138A>G
|
XP_011542690.1:p.Met380Val
|
|
XM_011544389.1:c.544A>G
|
XP_011542691.1:p.Met182Val
|
|
NM_001347705.1:c.661A>G
|
NP_001334634.1:p.Met221Val
|
|
NM_001347706.1:c.661A>G
|
NP_001334635.1:p.Met221Val
|
|
NM_001347707.1:c.544A>G
|
NP_001334636.1:p.Met182Val
|
|
NM_001347708.1:c.544A>G
|
NP_001334637.1:p.Met182Val
|
|
XM_011544389.2:c.544A>G
|
XP_011542691.1:p.Met182Val
|
|
NM_000742.4:c.1138A>G
MANE Select
|
NP_000733.2:p.Met380Val
|
|
NM_001282455.2:c.1093A>G
|
NP_001269384.1:p.Met365Val
|
|
NM_001347705.2:c.661A>G
|
NP_001334634.1:p.Met221Val
|
|
NM_001347706.2:c.661A>G
|
NP_001334635.1:p.Met221Val
|
|
NM_001347707.2:c.544A>G
|
NP_001334636.1:p.Met182Val
|
|
NM_001347708.2:c.544A>G
|
NP_001334637.1:p.Met182Val
|
|