ENST00000399503.4:c.3170T>G
MANE Select
|
ENSP00000382423.3:p.Ile1057Arg
|
|
ENST00000399503.3:c.3170T>G
|
ENSP00000382423.3:p.Ile1057Arg
|
|
NM_005921.1:c.3170T>G
|
NP_005912.1:p.Ile1057Arg
|
|
XM_005248519.3:c.2792T>G
|
XP_005248576.2:p.Ile931Arg
|
|
XM_011543406.1:c.2915T>G
|
XP_011541708.1:p.Ile972Arg
|
|
XM_011543407.1:c.2891T>G
|
XP_011541709.1:p.Ile964Arg
|
|
XM_011543408.1:c.3170T>G
|
XP_011541710.1:p.Ile1057Arg
|
|
XM_017009484.1:c.2759T>G
|
XP_016864973.1:p.Ile920Arg
|
|
XM_017009485.1:c.2681T>G
|
XP_016864974.1:p.Ile894Arg
|
|
XR_001742068.2:n.3201T>G
|
|
|
NM_005921.2:c.3170T>G
MANE Select
|
NP_005912.1:p.Ile1057Arg
|
|