ENST00000622290.5:c.3193T=
|
ENSP00000483331.2:p.Ser1065=
|
|
ENST00000205557.12:c.3193T=
MANE Select
|
ENSP00000205557.7:p.Ser1065=
|
|
ENST00000640696.1:c.208T=
|
ENSP00000492197.1:p.Ser70=
|
|
ENST00000205557.11:c.3193T=
|
ENSP00000205557.7:p.Ser1065=
|
|
ENST00000456970.6:c.3018T=
|
ENSP00000405002.2:n.3018T=
|
|
ENST00000622290.4:c.*402T=
|
ENSP00000483331.1:n.*402T=
|
|
NM_001171.5:c.3193T=
|
NP_001162.4:p.Ser1065=
|
|
XM_011522479.1:c.3160T=
|
XP_011520781.1:p.Ser1054=
|
|
XM_011522480.1:c.2851T=
|
XP_011520782.1:p.Ser951=
|
|
XM_011522481.1:c.2851T=
|
XP_011520783.1:p.Ser951=
|
|
XR_932836.1:n.3428T=
|
|
|
XR_932837.1:n.3429T=
|
|
|
XR_932838.1:n.3429T=
|
|
|
NM_001351800.1:c.2851T=
|
NP_001338729.1:p.Ser951=
|
|
NR_147784.1:n.3055T=
|
|
|
XM_011522479.2:c.3160T=
|
XP_011520781.1:p.Ser1054=
|
|
XM_011522481.3:c.2851T=
|
XP_011520783.1:p.Ser951=
|
|
XM_017023212.1:c.3025T=
|
XP_016878701.1:p.Ser1009=
|
|
XM_017023214.1:c.3193T=
|
XP_016878703.1:p.Ser1065=
|
|
XM_024450261.1:c.3229T=
|
XP_024306029.1:p.Ser1077=
|
|
XR_932836.2:n.3374T=
|
|
|
XR_932837.3:n.3374T=
|
|
|
XR_932838.3:n.3374T=
|
|
|
NM_001171.6:c.3193T=
MANE Select
|
NP_001162.5:p.Ser1065=
|
|