ENST00000374479.4:c.407C>A
MANE Select
|
ENSP00000363603.3:p.Thr136Lys
|
|
ENST00000374479.3:c.407C>A
|
ENSP00000363603.3:p.Thr136Lys
|
|
NM_000147.4:c.407C>A
|
NP_000138.2:p.Thr136Lys
|
|
XM_005245821.1:c.32C>A
|
XP_005245878.1:p.Thr11Lys
|
|
XM_011541167.1:c.-227C>A
|
XP_011539469.1:n.-227C>A
|
|
XM_005245821.3:c.32C>A
|
XP_005245878.1:p.Thr11Lys
|
|
XM_011541167.3:c.-227C>A
|
XP_011539469.1:n.-227C>A
|
|
XM_017000905.2:c.104C>A
|
XP_016856394.1:p.Thr35Lys
|
|
NM_000147.5:c.407C>A
MANE Select
|
NP_000138.2:p.Thr136Lys
|
|
NR_174379.1:n.585C>A
|
|
|
NR_174380.1:n.634C>A
|
|
|
NR_174381.1:n.473C>A
|
|
|
NR_174382.1:n.870C>A
|
|
|