ENST00000359595.8:c.434G=
MANE Select
|
ENSP00000352606.4:p.Arg145=
|
|
ENST00000359595.7:c.434G=
|
ENSP00000352606.3:p.Arg145=
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|
ENST00000558770.5:c.434G=
|
ENSP00000456458.1:p.Arg145=
|
|
ENST00000562281.1:c.434G=
|
ENSP00000456985.1:p.Arg145=
|
|
ENST00000562889.5:c.620G=
|
ENSP00000457180.1:p.Arg207=
|
|
ENST00000563808.1:n.536G=
|
|
|
NM_001307952.1:c.620G=
|
NP_001294881.1:p.Arg207=
|
|
NM_178232.2:c.434G=
|
NP_839946.1:p.Arg145=
|
|
NM_178232.3:c.434G=
|
NP_839946.1:p.Arg145=
|
|
XM_011521261.1:c.566G=
|
XP_011519563.1:p.Arg189=
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|
XR_243204.1:n.649G=
|
|
|
XR_931756.1:n.755G=
|
|
|
XM_017021934.2:c.620G=
|
XP_016877423.1:p.Arg207=
|
|
XM_017021935.2:c.55G=
|
XP_016877424.1:p.Ala19=
|
|
XM_017021936.2:c.55G=
|
XP_016877425.1:p.Ala19=
|
|
XR_001751098.2:n.767G=
|
|
|
XR_931756.3:n.768G=
|
|
|
NM_001307952.2:c.620G=
|
NP_001294881.1:p.Arg207=
|
|
NM_178232.4:c.434G=
MANE Select
|
NP_839946.1:p.Arg145=
|
|