ENST00000673913.2:c.1645C=
|
ENSP00000501161.2:p.Arg549=
|
|
ENST00000710286.1:c.2002C=
|
ENSP00000518176.1:p.Arg668=
|
|
ENST00000673903.1:c.1270C=
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ENSP00000501257.1:p.Arg424=
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|
ENST00000673913.1:c.385C=
|
ENSP00000501161.1:p.Arg129=
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|
ENST00000302118.5:c.1645C=
MANE Select
|
ENSP00000303208.5:p.Arg549=
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|
ENST00000490692.1:n.2227+980C=
|
|
|
NM_174936.3:c.1645C= , LRG_275t1:c.1645C=
|
NP_777596.2:p.Arg549=
|
|
NR_110451.1:n.1252C=
|
|
|
XM_011541193.1:c.766C=
|
XP_011539495.1:p.Arg256=
|
|
NM_174936.4:c.1645C=
MANE Select
|
NP_777596.2:p.Arg549=
|
|
NR_110451.2:n.1252C=
|
|
|