ENST00000399503.4:c.2577T>G
MANE Select
|
ENSP00000382423.3:p.Ile859Met
|
|
ENST00000399503.3:c.2577T>G
|
ENSP00000382423.3:p.Ile859Met
|
|
NM_005921.1:c.2577T>G
|
NP_005912.1:p.Ile859Met
|
|
XM_005248519.3:c.2199T>G
|
XP_005248576.2:p.Ile733Met
|
|
XM_011543406.1:c.2322T>G
|
XP_011541708.1:p.Ile774Met
|
|
XM_011543407.1:c.2298T>G
|
XP_011541709.1:p.Ile766Met
|
|
XM_011543408.1:c.2577T>G
|
XP_011541710.1:p.Ile859Met
|
|
XM_017009484.1:c.2166T>G
|
XP_016864973.1:p.Ile722Met
|
|
XM_017009485.1:c.2088T>G
|
XP_016864974.1:p.Ile696Met
|
|
XR_001742068.2:n.2608T>G
|
|
|
NM_005921.2:c.2577T>G
MANE Select
|
NP_005912.1:p.Ile859Met
|
|