ENST00000684241.1:n.1142G>T
|
|
|
ENST00000262186.10:c.309G>T
MANE Select
|
ENSP00000262186.5:p.Gly103=
|
|
ENST00000262186.9:c.309G>T
|
ENSP00000262186.5:p.Gly103=
|
|
ENST00000430723.4:c.132G>T
|
ENSP00000387657.4:p.Gly44=
|
|
ENST00000532957.5:n.532G>T
|
|
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NM_000238.3:c.309G>T , LRG_288t1:c.309G>T
|
NP_000229.1:p.Gly103=
|
|
NM_172056.2:c.309G>T , LRG_288t2:c.309G>T
|
NP_742053.1:p.Gly103=
|
|
XM_011516185.1:c.9G>T
|
XP_011514487.1:p.Gly3=
|
|
XM_011516186.1:c.309G>T
|
XP_011514488.1:p.Gly103=
|
|
XM_011516185.2:c.9G>T
|
XP_011514487.1:p.Gly3=
|
|
XM_011516186.3:c.309G>T
|
XP_011514488.1:p.Gly103=
|
|
XM_017012195.1:c.159G>T
|
XP_016867684.1:p.Gly53=
|
|
XM_017012196.1:c.132G>T
|
XP_016867685.1:p.Gly44=
|
|
NM_000238.4:c.309G>T
MANE Select
|
NP_000229.1:p.Gly103=
|
|