ENST00000426333.7:c.2087T>G
MANE Select
|
ENSP00000392094.1:p.Leu696Arg
|
|
ENST00000402521.7:c.1982T>G
|
ENSP00000385873.2:p.Leu661Arg
|
|
ENST00000426333.6:c.2087T>G
|
ENSP00000392094.1:p.Leu696Arg
|
|
ENST00000586276.5:n.1749T>G
|
|
|
ENST00000590124.5:c.89T>G
|
ENSP00000467249.1:p.Leu30Arg
|
|
ENST00000590367.5:n.1815T>G
|
|
|
ENST00000590977.5:n.695T>G
|
|
|
ENST00000591382.5:c.2087T>G
|
ENSP00000467805.1:p.Leu696Arg
|
|
ENST00000592576.5:c.2057T>G
|
ENSP00000465058.1:p.Leu686Arg
|
|
NM_001142605.1:c.1982T>G
|
NP_001136077.1:p.Leu661Arg
|
|
NM_001258353.1:c.2087T>G
|
NP_001245282.1:p.Leu696Arg
|
|
NM_001258354.1:c.2057T>G
|
NP_001245283.1:p.Leu686Arg
|
|
NM_004247.3:c.2087T>G
|
NP_004238.3:p.Leu696Arg
|
|
XR_934602.1:n.2172T>G
|
|
|
XR_934602.3:n.2168T>G
|
|
|
NM_004247.4:c.2087T>G
MANE Select
|
NP_004238.3:p.Leu696Arg
|
|
NM_001142605.2:c.1982T>G
|
NP_001136077.1:p.Leu661Arg
|
|
NM_001258353.2:c.2087T>G
|
NP_001245282.1:p.Leu696Arg
|
|
NM_001258354.2:c.2057T>G
|
NP_001245283.1:p.Leu686Arg
|
|