ENST00000333891.14:c.14536T=
MANE Select
|
ENSP00000334319.8:p.Ser4846=
|
|
ENST00000333891.13:c.14536T=
|
ENSP00000334319.8:p.Ser4846=
|
|
ENST00000423517.6:c.14536T=
|
ENSP00000388393.2:p.Ser4846=
|
|
ENST00000426442.6:n.1031T=
|
|
|
ENST00000618073.1:c.799T=
|
ENSP00000482390.1:p.Ser267=
|
|
NM_014510.2:c.14536T=
|
NP_055325.2:p.Ser4846=
|
|
NM_033026.5:c.14536T=
|
NP_149015.2:p.Ser4846=
|
|
XM_017012006.2:c.7441T=
|
XP_016867495.1:p.Ser2481=
|
|
XM_017012007.1:c.7414T=
|
XP_016867496.1:p.Ser2472=
|
|
XR_001744643.2:n.16105T=
|
|
|
NM_033026.6:c.14536T=
MANE Select
|
NP_149015.2:p.Ser4846=
|
|
NM_014510.3:c.14536T=
|
NP_055325.2:p.Ser4846=
|
|