ENST00000355265.7:c.526-44G>T
MANE Select
|
ENSP00000347409.2:n.526-44G>T
|
|
ENST00000467543.6:c.*378-44G>T
|
ENSP00000420011.2:n.*378-44G>T
|
|
ENST00000355265.6:c.526-44G>T
|
ENSP00000347409.2:n.526-44G>T
|
|
ENST00000467543.5:c.469-44G>T
|
ENSP00000420011.1:n.469-44G>T
|
|
ENST00000476829.5:c.525+287G>T
|
ENSP00000419889.1:n.525+287G>T
|
|
ENST00000479768.6:n.644-44G>T
|
|
|
ENST00000494148.1:n.125-44G>T
|
|
|
NM_000420.2:c.526-44G>T
|
NP_000411.1:n.526-44G>T
|
|
XM_005249993.2:c.562-44G>T
|
XP_005250050.1:n.562-44G>T
|
|
NM_000420.3:c.526-44G>T
MANE Select
|
NP_000411.1:n.526-44G>T
|
|