ENST00000267845.8:c.1757G>C
MANE Select
|
ENSP00000267845.3:p.Ser586Thr
|
|
ENST00000267845.7:c.1757G>C
|
ENSP00000267845.3:p.Ser586Thr
|
|
ENST00000543581.5:c.1658G>C
|
ENSP00000440252.1:p.Ser553Thr
|
|
ENST00000559816.1:n.1501G>C
|
|
|
NM_001306146.1:c.1658G>C
|
NP_001293075.1:p.Ser553Thr
|
|
NM_002112.3:c.1757G>C
|
NP_002103.2:p.Ser586Thr
|
|
XM_011521479.1:c.1520G>C
|
XP_011519781.1:p.Ser507Thr
|
|
XM_011521480.1:c.1325G>C
|
XP_011519782.1:p.Ser442Thr
|
|
XM_017022094.1:c.1862G>C
|
XP_016877583.1:p.Ser621Thr
|
|
XM_017022095.1:c.1763G>C
|
XP_016877584.1:p.Ser588Thr
|
|
XM_017022096.1:c.1634G>C
|
XP_016877585.1:p.Ser545Thr
|
|
XM_017022097.1:c.1625G>C
|
XP_016877586.1:p.Ser542Thr
|
|
XM_017022098.1:c.1430G>C
|
XP_016877587.1:p.Ser477Thr
|
|
NM_002112.4:c.1757G>C
MANE Select
|
NP_002103.2:p.Ser586Thr
|
|
NM_001306146.2:c.1658G>C
|
NP_001293075.1:p.Ser553Thr
|
|