ENST00000333891.14:c.14436C=
MANE Select
|
ENSP00000334319.8:p.Ser4812=
|
|
ENST00000333891.13:c.14436C=
|
ENSP00000334319.8:p.Ser4812=
|
|
ENST00000423517.6:c.14436C=
|
ENSP00000388393.2:p.Ser4812=
|
|
ENST00000426442.6:n.931C=
|
|
|
ENST00000618073.1:c.699C=
|
ENSP00000482390.1:p.Ser233=
|
|
NM_014510.2:c.14436C=
|
NP_055325.2:p.Ser4812=
|
|
NM_033026.5:c.14436C=
|
NP_149015.2:p.Ser4812=
|
|
XM_017012006.2:c.7341C=
|
XP_016867495.1:p.Ser2447=
|
|
XM_017012007.1:c.7314C=
|
XP_016867496.1:p.Ser2438=
|
|
XR_001744643.2:n.16005C=
|
|
|
NM_033026.6:c.14436C=
MANE Select
|
NP_149015.2:p.Ser4812=
|
|
NM_014510.3:c.14436C=
|
NP_055325.2:p.Ser4812=
|
|