ENST00000573725.2:c.6510G>T
|
ENSP00000460849.2:p.Leu2170=
|
|
ENST00000703537.1:c.2438G>T
|
|
|
ENST00000703538.1:c.*6413G>T
|
ENSP00000515361.1:n.*6413G>T
|
|
ENST00000703539.1:n.3004G>T
|
|
|
ENST00000703540.1:c.6543G>T
|
ENSP00000515362.1:p.Leu2181=
|
|
ENST00000703541.1:c.6555G>T
|
ENSP00000515363.1:p.Leu2185=
|
|
ENST00000304992.11:c.6690G>T
MANE Select
|
ENSP00000304350.6:p.Leu2230=
|
|
ENST00000304992.10:c.6690G>T
|
ENSP00000304350.6:p.Leu2230=
|
|
ENST00000572621.5:c.6690G>T
|
ENSP00000460348.1:p.Leu2230=
|
|
ENST00000572723.1:n.679G>T
|
|
|
NM_006445.3:c.6690G>T
|
NP_006436.3:p.Leu2230=
|
|
XM_024450537.1:c.6690G>T
|
XP_024306305.1:p.Leu2230=
|
|
NM_006445.4:c.6690G>T
MANE Select
|
NP_006436.3:p.Leu2230=
|
|