ENST00000355265.7:c.656A>T
MANE Select
|
ENSP00000347409.2:p.His219Leu
|
|
ENST00000467543.6:c.*508A>T
|
ENSP00000420011.2:n.*508A>T
|
|
ENST00000355265.6:c.656A>T
|
ENSP00000347409.2:p.His219Leu
|
|
ENST00000467543.5:c.599A>T
|
ENSP00000420011.1:p.His200Leu
|
|
ENST00000476829.5:c.525+461A>T
|
ENSP00000419889.1:n.525+461A>T
|
|
ENST00000479768.6:n.774A>T
|
|
|
ENST00000494148.1:n.255A>T
|
|
|
NM_000420.2:c.656A>T
|
NP_000411.1:p.His219Leu
|
|
XM_005249993.2:c.692A>T
|
XP_005250050.1:p.His231Leu
|
|
NM_000420.3:c.656A>T
MANE Select
|
NP_000411.1:p.His219Leu
|
|