ENST00000336112.9:c.3830G>C
|
ENSP00000337250.5:p.Arg1277Thr
|
|
ENST00000435504.9:c.3833G>C
MANE Select
|
ENSP00000391447.3:p.Arg1278Thr
|
|
ENST00000336112.8:c.3749G>C
|
ENSP00000337250.4:p.Arg1250Thr
|
|
ENST00000404843.5:c.2282G>C
|
ENSP00000383920.1:p.Arg761Thr
|
|
ENST00000435504.8:c.3833G>C
|
ENSP00000391447.3:p.Arg1278Thr
|
|
NM_018263.4:c.3833G>C
|
NP_060733.4:p.Arg1278Thr
|
|
XM_006712039.2:c.3467G>C
|
XP_006712102.1:p.Arg1156Thr
|
|
XM_006712040.1:c.3053G>C
|
XP_006712103.1:p.Arg1018Thr
|
|
XM_011532950.1:c.3830G>C
|
XP_011531252.1:p.Arg1277Thr
|
|
XM_011532951.1:c.3659G>C
|
XP_011531253.1:p.Arg1220Thr
|
|
NM_018263.5:c.3833G>C
|
NP_060733.4:p.Arg1278Thr
|
|
XM_006712039.3:c.3467G>C
|
XP_006712102.1:p.Arg1156Thr
|
|
XM_006712040.2:c.3053G>C
|
XP_006712103.1:p.Arg1018Thr
|
|
XM_011532950.3:c.3830G>C
|
XP_011531252.1:p.Arg1277Thr
|
|
XM_011532951.2:c.3659G>C
|
XP_011531253.1:p.Arg1220Thr
|
|
XM_017004430.1:c.3053G>C
|
XP_016859919.1:p.Arg1018Thr
|
|
XM_024452974.1:c.4013G>C
|
XP_024308742.1:p.Arg1338Thr
|
|
NM_001369346.1:c.3659G>C
|
NP_001356275.1:p.Arg1220Thr
|
|
NM_001369347.1:c.3053G>C
|
NP_001356276.1:p.Arg1018Thr
|
|
NM_018263.6:c.3833G>C
MANE Select
|
NP_060733.4:p.Arg1278Thr
|
|