ENST00000673913.2:c.1548G=
|
ENSP00000501161.2:p.Gly516=
|
|
ENST00000710286.1:c.1905G=
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ENSP00000518176.1:p.Gly635=
|
|
ENST00000673903.1:c.1173G=
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ENSP00000501257.1:p.Gly391=
|
|
ENST00000673913.1:c.288G=
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ENSP00000501161.1:p.Gly96=
|
|
ENST00000302118.5:c.1548G=
MANE Select
|
ENSP00000303208.5:p.Gly516=
|
|
ENST00000490692.1:n.2227+883G=
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|
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NM_174936.3:c.1548G= , LRG_275t1:c.1548G=
|
NP_777596.2:p.Gly516=
|
|
NR_110451.1:n.1155G=
|
|
|
XM_011541193.1:c.669G=
|
XP_011539495.1:p.Gly223=
|
|
NM_174936.4:c.1548G=
MANE Select
|
NP_777596.2:p.Gly516=
|
|
NR_110451.2:n.1155G=
|
|
|