ENST00000475778.2:n.725G=
|
|
|
ENST00000683214.1:n.544+14038G=
|
|
|
ENST00000684143.1:c.299G=
|
ENSP00000508264.1:p.Ser100=
|
|
ENST00000379374.5:c.299G=
MANE Select
|
ENSP00000368682.4:p.Ser100=
|
|
ENST00000379374.4:c.299G=
|
ENSP00000368682.4:p.Ser100=
|
|
NM_000444.5:c.299G=
|
NP_000435.3:p.Ser100=
|
|
NM_001282754.1:c.299G=
|
NP_001269683.1:p.Ser100=
|
|
XM_011545535.1:c.299G=
|
XP_011543837.1:p.Ser100=
|
|
XM_024452390.1:c.8G=
|
XP_024308158.1:p.Ser3=
|
|
XR_001755695.1:n.978G=
|
|
|
NM_000444.6:c.299G=
MANE Select
|
NP_000435.3:p.Ser100=
|
|
NM_001282754.2:c.299G=
|
NP_001269683.1:p.Ser100=
|
|