|
NM_032119.4:c.18336T>G
MANE Select
|
NP_115495.3:p.Phe6112Leu
|
|
ENST00000405460.9:c.18336T>G
MANE Select
|
ENSP00000384582.2:p.Phe6112Leu
|
|
NM_032119.3:c.18336T>G
|
NP_115495.3:p.Phe6112Leu
|
|
NR_003149.1:n.18349T>G
|
|
|
NR_003149.2:n.18352T>G
|
|
|
ENST00000405460.6:c.18336T>G
|
ENSP00000384582.2:p.Phe6112Leu
|
|
ENST00000425867.2:c.5319T>G
|
ENSP00000392618.2:p.Phe1773Leu
|
|
ENST00000425867.3:c.7290T>G
|
ENSP00000392618.3:p.Phe2430Leu
|
|
ENST00000638510.1:n.5603T>G
|
|
|
ENST00000638990.1:c.1548T>G
|
|
|
ENST00000639212.1:n.256T>G
|
|
|
ENST00000639530.1:n.204T>G
|
|
|
ENST00000639821.1:c.420T>G
|
ENSP00000492216.1:p.Phe140Leu
|
|
ENST00000640256.1:n.204T>G
|
|
|
ENST00000640407.1:c.4785T>G
|
ENSP00000491425.1:n.4785T>G
|
|
ENST00000640815.1:c.420T>G
|
ENSP00000491767.1:p.Phe140Leu
|
|
XM_011543675.1:c.18333T>G
|
XP_011541977.1:p.Phe6111Leu
|
|
XM_011543676.1:c.18255T>G
|
XP_011541978.1:p.Phe6085Leu
|
|
XM_011543677.1:c.15639T>G
|
XP_011541979.1:p.Phe5213Leu
|
|
XM_017009963.2:c.18357T>G
|
XP_016865452.1:p.Phe6119Leu
|
|
XM_017009964.2:c.18354T>G
|
XP_016865453.1:p.Phe6118Leu
|
|
XM_017009965.1:c.18354T>G
|
XP_016865454.1:p.Phe6118Leu
|
|
XM_017009966.2:c.18276T>G
|
XP_016865455.1:p.Phe6092Leu
|
|
XM_017009967.1:c.18261T>G
|
XP_016865456.1:p.Phe6087Leu
|
|
XM_017009968.2:c.18177T>G
|
XP_016865457.1:p.Phe6059Leu
|
|
XM_017009969.2:c.18357T>G
|
XP_016865458.1:p.Phe6119Leu
|
|
XM_017009972.1:c.11475T>G
|
XP_016865461.1:p.Phe3825Leu
|
|
XM_017009973.1:c.11454T>G
|
XP_016865462.1:p.Phe3818Leu
|