ENST00000673913.2:c.*115G=
|
ENSP00000501161.2:n.*115G=
|
|
ENST00000710286.1:c.2132G=
|
ENSP00000518176.1:p.Arg711=
|
|
ENST00000673903.1:c.1400G=
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ENSP00000501257.1:p.Arg467=
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|
ENST00000673913.1:c.625G=
|
ENSP00000501161.1:n.625G=
|
|
ENST00000302118.5:c.1775G=
MANE Select
|
ENSP00000303208.5:p.Arg592=
|
|
ENST00000490692.1:n.2321G=
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|
|
NM_174936.3:c.1775G= , LRG_275t1:c.1775G=
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NP_777596.2:p.Arg592=
|
|
NR_110451.1:n.1382G=
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|
|
XM_011541193.1:c.896G=
|
XP_011539495.1:p.Arg299=
|
|
NM_174936.4:c.1775G=
MANE Select
|
NP_777596.2:p.Arg592=
|
|
NR_110451.2:n.1382G=
|
|
|