ENST00000684241.1:n.1836C=
|
|
|
ENST00000262186.10:c.1003C=
MANE Select
|
ENSP00000262186.5:p.Gln335=
|
|
ENST00000262186.9:c.1003C=
|
ENSP00000262186.5:p.Gln335=
|
|
ENST00000430723.4:c.655C=
|
ENSP00000387657.4:p.Gln219=
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|
ENST00000532957.5:n.1226C=
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|
|
NM_000238.3:c.1003C= , LRG_288t1:c.1003C=
|
NP_000229.1:p.Gln335=
|
|
NM_172056.2:c.1003C= , LRG_288t2:c.1003C=
|
NP_742053.1:p.Gln335=
|
|
XM_011516185.1:c.703C=
|
XP_011514487.1:p.Gln235=
|
|
XM_011516186.1:c.1003C=
|
XP_011514488.1:p.Gln335=
|
|
XM_011516185.2:c.703C=
|
XP_011514487.1:p.Gln235=
|
|
XM_011516186.3:c.1003C=
|
XP_011514488.1:p.Gln335=
|
|
XM_017012195.1:c.853C=
|
XP_016867684.1:p.Gln285=
|
|
XM_017012196.1:c.826C=
|
XP_016867685.1:p.Gln276=
|
|
NM_000238.4:c.1003C=
MANE Select
|
NP_000229.1:p.Gln335=
|
|