ENST00000399503.4:c.3014G>C
MANE Select
|
ENSP00000382423.3:p.Arg1005Thr
|
|
ENST00000399503.3:c.3014G>C
|
ENSP00000382423.3:p.Arg1005Thr
|
|
NM_005921.1:c.3014G>C
|
NP_005912.1:p.Arg1005Thr
|
|
XM_005248519.3:c.2636G>C
|
XP_005248576.2:p.Arg879Thr
|
|
XM_011543406.1:c.2759G>C
|
XP_011541708.1:p.Arg920Thr
|
|
XM_011543407.1:c.2735G>C
|
XP_011541709.1:p.Arg912Thr
|
|
XM_011543408.1:c.3014G>C
|
XP_011541710.1:p.Arg1005Thr
|
|
XM_017009484.1:c.2603G>C
|
XP_016864973.1:p.Arg868Thr
|
|
XM_017009485.1:c.2525G>C
|
XP_016864974.1:p.Arg842Thr
|
|
XR_001742068.2:n.3045G>C
|
|
|
NM_005921.2:c.3014G>C
MANE Select
|
NP_005912.1:p.Arg1005Thr
|
|