ENST00000684241.1:n.3940G=
|
|
|
ENST00000262186.10:c.3107G=
MANE Select
|
ENSP00000262186.5:p.Gly1036=
|
|
ENST00000330883.9:c.2087G=
|
ENSP00000328531.4:p.Gly696=
|
|
ENST00000262186.9:c.3107G=
|
ENSP00000262186.5:p.Gly1036=
|
|
ENST00000330883.8:c.2087G=
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ENSP00000328531.4:p.Gly696=
|
|
NM_000238.3:c.3107G= , LRG_288t1:c.3107G=
|
NP_000229.1:p.Gly1036=
|
|
NM_172057.2:c.2087G= , LRG_288t3:c.2087G=
|
NP_742054.1:p.Gly696=
|
|
XM_011516185.1:c.2807G=
|
XP_011514487.1:p.Gly936=
|
|
XM_011516185.2:c.2807G=
|
XP_011514487.1:p.Gly936=
|
|
XM_017012195.1:c.2957G=
|
XP_016867684.1:p.Gly986=
|
|
XM_017012196.1:c.2930G=
|
XP_016867685.1:p.Gly977=
|
|
NM_000238.4:c.3107G=
MANE Select
|
NP_000229.1:p.Gly1036=
|
|
NM_172057.3:c.2087G=
|
NP_742054.1:p.Gly696=
|
|