ENST00000355265.7:c.616T>C
MANE Select
|
ENSP00000347409.2:p.Phe206Leu
|
|
ENST00000467543.6:c.*468T>C
|
ENSP00000420011.2:n.*468T>C
|
|
ENST00000355265.6:c.616T>C
|
ENSP00000347409.2:p.Phe206Leu
|
|
ENST00000467543.5:c.559T>C
|
ENSP00000420011.1:p.Phe187Leu
|
|
ENST00000476829.5:c.525+421T>C
|
ENSP00000419889.1:n.525+421T>C
|
|
ENST00000479768.6:n.734T>C
|
|
|
ENST00000494148.1:n.215T>C
|
|
|
NM_000420.2:c.616T>C
|
NP_000411.1:p.Phe206Leu
|
|
XM_005249993.2:c.652T>C
|
XP_005250050.1:p.Phe218Leu
|
|
NM_000420.3:c.616T>C
MANE Select
|
NP_000411.1:p.Phe206Leu
|
|