ENST00000374552.9:c.441T>G
MANE Select
|
ENSP00000363680.4:p.Ser147=
|
|
ENST00000374548.5:n.683T>G
|
|
|
ENST00000374552.8:c.441T>G
|
ENSP00000363680.4:p.Ser147=
|
|
ENST00000374553.6:c.441T>G
|
ENSP00000363681.2:p.Ser147=
|
|
ENST00000502251.5:n.734T>G
|
|
|
ENST00000503592.5:c.45T>G
|
ENSP00000423037.1:p.Ser15=
|
|
ENST00000524573.5:c.441T>G
|
ENSP00000432585.1:p.Ser147=
|
|
ENST00000533317.5:n.1056T>G
|
|
|
ENST00000616899.1:c.45T>G
|
ENSP00000481963.1:p.Ser15=
|
|
NM_001005609.1:c.441T>G
|
NP_001005609.1:p.Ser147=
|
|
NM_001005612.2:c.441T>G
|
NP_001005612.2:p.Ser147=
|
|
NM_001399.4:c.441T>G
|
NP_001390.1:p.Ser147=
|
|
XM_006724630.2:c.441T>G
|
XP_006724693.1:p.Ser147=
|
|
XM_011530885.1:c.441T>G
|
XP_011529187.1:p.Ser147=
|
|
XM_011530885.2:c.441T>G
|
XP_011529187.1:p.Ser147=
|
|
XM_017029336.1:c.441T>G
|
XP_016884825.1:p.Ser147=
|
|
NM_001399.5:c.441T>G
MANE Select
|
NP_001390.1:p.Ser147=
|
|
NM_001005609.2:c.441T>G
|
NP_001005609.1:p.Ser147=
|
|
NM_001005612.3:c.441T>G
|
NP_001005612.2:p.Ser147=
|
|