ENST00000315491.12:c.854C>G
MANE Select
|
ENSP00000320295.7:p.Thr285Ser
|
|
ENST00000680788.1:n.4275C>G
|
|
|
ENST00000315491.11:c.854C>G
|
ENSP00000320295.7:p.Thr285Ser
|
|
ENST00000554444.5:c.638C>G
|
ENSP00000451617.1:p.Thr213Ser
|
|
ENST00000555576.5:c.277+1727C>G
|
ENSP00000452554.1:n.277+1727C>G
|
|
ENST00000555609.5:c.*939C>G
|
ENSP00000451276.1:n.*939C>G
|
|
ENST00000556922.1:c.1895C>G
|
ENSP00000451560.1:p.Thr632Ser
|
|
NM_001197181.1:c.638C>G
|
NP_001184110.1:p.Thr213Ser
|
|
NM_006086.3:c.854C>G
|
NP_006077.2:p.Thr285Ser
|
|
NM_006086.4:c.854C>G
MANE Select
|
NP_006077.2:p.Thr285Ser
|
|
NM_001197181.2:c.638C>G
|
NP_001184110.1:p.Thr213Ser
|
|