ENST00000703783.1:n.343C>G
|
|
|
ENST00000703785.1:n.424C>G
|
|
|
ENST00000262464.9:c.3559C>G
MANE Select
|
ENSP00000262464.4:p.Leu1187Val
|
|
ENST00000262464.8:c.3559C>G
|
ENSP00000262464.4:p.Leu1187Val
|
|
ENST00000507835.5:c.109C>G
|
ENSP00000426839.1:p.Leu37Val
|
|
ENST00000508053.5:c.3559C>G
|
ENSP00000424571.1:p.Leu1187Val
|
|
ENST00000508989.5:c.3460C>G
|
ENSP00000425596.1:p.Leu1154Val
|
|
ENST00000619499.4:c.3556C>G
|
ENSP00000482132.1:p.Leu1186Val
|
|
NM_001999.3:c.3559C>G
|
NP_001990.2:p.Leu1187Val
|
|
XM_017009228.2:c.3406C>G
|
XP_016864717.1:p.Leu1136Val
|
|
NM_001999.4:c.3559C>G
MANE Select
|
NP_001990.2:p.Leu1187Val
|
|