ENST00000703783.1:n.286C>T
|
|
|
ENST00000703785.1:n.367C>T
|
|
|
ENST00000262464.9:c.3502C>T
MANE Select
|
ENSP00000262464.4:p.Leu1168Phe
|
|
ENST00000262464.8:c.3502C>T
|
ENSP00000262464.4:p.Leu1168Phe
|
|
ENST00000507835.5:c.52C>T
|
ENSP00000426839.1:p.Leu18Phe
|
|
ENST00000508053.5:c.3502C>T
|
ENSP00000424571.1:p.Leu1168Phe
|
|
ENST00000508989.5:c.3403C>T
|
ENSP00000425596.1:p.Leu1135Phe
|
|
ENST00000619499.4:c.3499C>T
|
ENSP00000482132.1:p.Leu1167Phe
|
|
NM_001999.3:c.3502C>T
|
NP_001990.2:p.Leu1168Phe
|
|
XM_017009228.2:c.3349C>T
|
XP_016864717.1:p.Leu1117Phe
|
|
NM_001999.4:c.3502C>T
MANE Select
|
NP_001990.2:p.Leu1168Phe
|
|