ENST00000389857.11:c.5216C>G
MANE Select
|
ENSP00000374507.6:p.Thr1739Ser
|
|
ENST00000331194.8:c.788C>G
|
ENSP00000330332.8:p.Thr263Ser
|
|
ENST00000334448.5:n.1028C>G
|
|
|
ENST00000389857.10:c.5216C>G
|
ENSP00000374507.6:p.Thr1739Ser
|
|
ENST00000556726.5:c.1444C>G
|
|
|
NM_001080414.3:c.5216C>G
|
NP_001073883.2:p.Thr1739Ser
|
|
XM_011536796.1:c.5108C>G
|
XP_011535098.1:p.Thr1703Ser
|
|
XR_429316.2:n.5491C>G
|
|
|
XM_011536796.2:c.5108C>G
|
XP_011535098.1:p.Thr1703Ser
|
|
XM_017021336.1:c.2297C>G
|
XP_016876825.1:p.Thr766Ser
|
|
XR_429316.4:n.5489C>G
|
|
|
NM_001080414.4:c.5216C>G
MANE Select
|
NP_001073883.2:p.Thr1739Ser
|
|