ENST00000399503.4:c.3041T>G
MANE Select
|
ENSP00000382423.3:p.Ile1014Arg
|
|
ENST00000399503.3:c.3041T>G
|
ENSP00000382423.3:p.Ile1014Arg
|
|
NM_005921.1:c.3041T>G
|
NP_005912.1:p.Ile1014Arg
|
|
XM_005248519.3:c.2663T>G
|
XP_005248576.2:p.Ile888Arg
|
|
XM_011543406.1:c.2786T>G
|
XP_011541708.1:p.Ile929Arg
|
|
XM_011543407.1:c.2762T>G
|
XP_011541709.1:p.Ile921Arg
|
|
XM_011543408.1:c.3041T>G
|
XP_011541710.1:p.Ile1014Arg
|
|
XM_017009484.1:c.2630T>G
|
XP_016864973.1:p.Ile877Arg
|
|
XM_017009485.1:c.2552T>G
|
XP_016864974.1:p.Ile851Arg
|
|
XR_001742068.2:n.3072T>G
|
|
|
NM_005921.2:c.3041T>G
MANE Select
|
NP_005912.1:p.Ile1014Arg
|
|