ENST00000382103.7:c.944C>G
MANE Select
|
ENSP00000371535.2:p.Ser315Ter
|
|
ENST00000680581.1:c.944C>G
|
ENSP00000506483.1:p.Ser315Ter
|
|
ENST00000680824.1:n.2160C>G
|
|
|
ENST00000681071.1:n.1236C>G
|
|
|
ENST00000681341.1:n.2085C>G
|
|
|
ENST00000681948.1:c.1199C>G
|
ENSP00000505991.1:p.Ser400Ter
|
|
ENST00000358971.7:c.*742C>G
|
ENSP00000351857.3:n.*742C>G
|
|
ENST00000382103.6:c.944C>G
|
ENSP00000371535.2:p.Ser315Ter
|
|
ENST00000503150.1:c.226C>G
|
|
|
ENST00000505513.1:n.244C>G
|
|
|
ENST00000514585.5:c.*645C>G
|
ENSP00000421880.1:n.*645C>G
|
|
NM_016955.3:c.944C>G
|
NP_058651.3:p.Ser315Ter
|
|
XM_005248168.2:c.707C>G
|
XP_005248225.1:p.Ser236Ter
|
|
XM_006713965.2:c.764C>G
|
XP_006714028.1:p.Ser255Ter
|
|
XM_011513846.1:c.941C>G
|
XP_011512148.1:p.Ser314Ter
|
|
XM_011513847.1:c.911C>G
|
XP_011512149.1:p.Ser304Ter
|
|
XM_011513848.1:c.764C>G
|
XP_011512150.1:p.Ser255Ter
|
|
XM_011513846.2:c.941C>G
|
XP_011512148.1:p.Ser314Ter
|
|
XM_011513847.2:c.911C>G
|
XP_011512149.1:p.Ser304Ter
|
|
XM_017008277.1:c.1199C>G
|
XP_016863766.1:p.Ser400Ter
|
|
XM_017008278.1:c.521C>G
|
XP_016863767.1:p.Ser174Ter
|
|
NM_016955.4:c.944C>G
MANE Select
|
NP_058651.3:p.Ser315Ter
|
|