ENST00000647720.2:c.*68G>T
|
ENSP00000497673.2:n.*68G>T
|
|
ENST00000647978.2:c.*3573G>T
|
ENSP00000497658.1:n.*3573G>T
|
|
ENST00000649781.2:c.3676G>T
|
ENSP00000497203.1:p.Gly1226Ter
|
|
ENST00000685018.2:c.3859G>T
|
ENSP00000510194.2:p.Gly1287Ter
|
|
ENST00000687278.2:c.*512G>T
|
ENSP00000509593.2:n.*512G>T
|
|
ENST00000699585.1:c.*68G>T
|
ENSP00000514456.1:n.*68G>T
|
|
ENST00000699598.1:c.3859G>T
|
ENSP00000514467.1:p.Gly1287Ter
|
|
ENST00000699599.1:c.3859G>T
|
ENSP00000514468.1:p.Gly1287Ter
|
|
ENST00000699600.1:c.*520G>T
|
ENSP00000514469.1:n.*520G>T
|
|
ENST00000699601.1:c.*2234G>T
|
ENSP00000514470.1:n.*2234G>T
|
|
ENST00000699602.1:c.3853G>T
|
ENSP00000514471.1:p.Gly1285Ter
|
|
ENST00000699604.1:c.*3683G>T
|
ENSP00000514472.1:n.*3683G>T
|
|
ENST00000699605.1:c.3433G>T
|
ENSP00000514473.1:p.Gly1145Ter
|
|
ENST00000685018.1:c.607G>T
|
ENSP00000510194.1:p.Gly203Ter
|
|
ENST00000687278.1:c.1646G>T
|
ENSP00000509593.1:n.1646G>T
|
|
ENST00000689011.1:c.441G>T
|
|
|
ENST00000003084.11:c.3859G>T
MANE Select
|
ENSP00000003084.6:p.Gly1287Ter
|
|
ENST00000647720.1:c.1309G>T
|
|
|
ENST00000649781.1:c.3676G>T
|
ENSP00000497203.1:p.Gly1226Ter
|
|
ENST00000003084.10:c.3859G>T
|
ENSP00000003084.6:p.Gly1287Ter
|
|
ENST00000426809.5:c.3769G>T
|
ENSP00000389119.1:p.Gly1257Ter
|
|
NM_000492.3:c.3859G>T , LRG_663t1:c.3859G>T
|
NP_000483.3:p.Gly1287Ter
|
|
XM_011515751.1:c.3949G>T
|
XP_011514053.1:p.Gly1317Ter
|
|
XM_011515752.1:c.3949G>T
|
XP_011514054.1:p.Gly1317Ter
|
|
XM_011515753.1:c.3616G>T
|
XP_011514055.1:p.Gly1206Ter
|
|
XM_011515754.1:c.3616G>T
|
XP_011514056.1:p.Gly1206Ter
|
|
NM_000492.4:c.3859G>T
MANE Select
|
NP_000483.3:p.Gly1287Ter
|
|