ENST00000560229.6:n.39G=
|
|
|
ENST00000562833.2:c.1351-287G=
|
ENSP00000454786.2:n.1351-287G=
|
|
ENST00000642270.1:c.1358-287G=
|
ENSP00000496443.1:n.1358-287G=
|
|
ENST00000647841.1:c.3+7G=
MANE Select
|
ENSP00000498019.1:n.3+7G=
|
|
ENST00000330244.10:c.3+7G=
|
ENSP00000346046.5:n.3+7G=
|
|
ENST00000558397.1:c.3+7G=
|
ENSP00000452889.1:n.3+7G=
|
|
ENST00000559273.1:n.31+7G=
|
|
|
ENST00000559776.1:n.1G=
|
|
|
ENST00000560229.5:n.39G=
|
|
|
ENST00000560639.1:n.27+7G=
|
|
|
ENST00000561157.5:c.3+7G=
|
ENSP00000453910.1:n.3+7G=
|
|
ENST00000562833.1:c.780-287G=
|
|
|
NM_001021.4:c.3+7G=
|
NP_001012.1:n.3+7G=
|
|
NR_111943.1:n.39G=
|
|
|
NR_111944.1:n.119+7G=
|
|
|
NM_001021.6:c.3+7G=
MANE Select
|
NP_001012.1:n.3+7G=
|
|
NR_111944.2:n.139+7G=
|
|
|
NR_111943.2:n.39G=
|
|
|
NR_111944.3:n.32+7G=
|
|
|