ENST00000282516.13:c.4757G>C
MANE Select
|
ENSP00000282516.8:p.Ser1586Thr
|
|
ENST00000652901.1:c.4757G>C
|
ENSP00000499536.1:p.Ser1586Thr
|
|
ENST00000282516.12:c.4757G>C
|
ENSP00000282516.8:p.Ser1586Thr
|
|
ENST00000448238.2:c.4757G>C
|
ENSP00000406266.2:p.Ser1586Thr
|
|
ENST00000621733.1:c.1-48427G>C
|
ENSP00000480694.1:n.1-48427G>C
|
|
NM_015384.4:c.4757G>C
|
NP_056199.2:p.Ser1586Thr
|
|
NM_133433.3:c.4757G>C
|
NP_597677.2:p.Ser1586Thr
|
|
XM_005248280.2:c.4757G>C
|
XP_005248337.1:p.Ser1586Thr
|
|
XM_005248282.3:c.4013G>C
|
XP_005248339.2:p.Ser1338Thr
|
|
XM_006714467.2:c.4757G>C
|
XP_006714530.1:p.Ser1586Thr
|
|
XM_006714468.1:c.4559G>C
|
XP_006714531.1:p.Ser1520Thr
|
|
XM_011514014.1:c.4376G>C
|
XP_011512316.1:p.Ser1459Thr
|
|
XM_011514015.1:c.4757G>C
|
XP_011512317.1:p.Ser1586Thr
|
|
XM_005248280.3:c.4757G>C
|
XP_005248337.1:p.Ser1586Thr
|
|
XM_005248282.5:c.4097G>C
|
XP_005248339.3:p.Ser1366Thr
|
|
XM_006714468.2:c.4559G>C
|
XP_006714531.1:p.Ser1520Thr
|
|
XM_017009329.1:c.4757G>C
|
XP_016864818.1:p.Ser1586Thr
|
|
XM_017009330.2:c.3140G>C
|
XP_016864819.1:p.Ser1047Thr
|
|
XM_017009331.1:c.3131G>C
|
XP_016864820.1:p.Ser1044Thr
|
|
NM_133433.4:c.4757G>C
MANE Select
|
NP_597677.2:p.Ser1586Thr
|
|
NM_015384.5:c.4757G>C
|
NP_056199.2:p.Ser1586Thr
|
|