ENST00000319429.7:n.599C>G
|
|
|
ENST00000398004.4:c.356C>G
MANE Select
|
ENSP00000381089.2:p.Thr119Ser
|
|
ENST00000673712.1:c.356C>G
|
ENSP00000501065.1:p.Thr119Ser
|
|
ENST00000674096.1:c.356C>G
|
ENSP00000501130.1:p.Thr119Ser
|
|
ENST00000398004.3:c.356C>G
|
ENSP00000381089.2:p.Thr119Ser
|
|
NM_018656.2:c.356C>G
|
NP_061126.2:p.Thr119Ser
|
|
XM_005269006.2:c.356C>G
|
XP_005269063.1:p.Thr119Ser
|
|
NM_001354997.1:c.356C>G
|
NP_001341926.1:p.Thr119Ser
|
|
NM_001354998.1:c.356C>G
|
NP_001341927.1:p.Thr119Ser
|
|
NM_018656.3:c.356C>G
|
NP_061126.2:p.Thr119Ser
|
|
NR_149143.1:n.648C>G
|
|
|
NR_149144.1:n.648C>G
|
|
|
NM_001354997.3:c.356C>G
|
NP_001341926.1:p.Thr119Ser
|
|
NM_001354998.2:c.356C>G
|
NP_001341927.1:p.Thr119Ser
|
|
NM_018656.5:c.356C>G
MANE Select
|
NP_061126.2:p.Thr119Ser
|
|
NR_149143.3:n.558C>G
|
|
|
NR_149144.3:n.558C>G
|
|
|