ENST00000405460.9:c.11513T>G
MANE Select
|
ENSP00000384582.2:p.Leu3838Trp
|
|
ENST00000425867.3:c.644T>G
|
ENSP00000392618.3:p.Leu215Trp
|
|
ENST00000639431.1:c.265+78909T>G
|
ENSP00000491057.1:n.265+78909T>G
|
|
ENST00000640374.1:n.4657T>G
|
|
|
ENST00000640464.1:n.1932T>G
|
|
|
ENST00000405460.6:c.11513T>G
|
ENSP00000384582.2:p.Leu3838Trp
|
|
ENST00000509621.1:c.4210T>G
|
|
|
NM_032119.3:c.11513T>G
|
NP_115495.3:p.Leu3838Trp
|
|
NR_003149.1:n.11526T>G
|
|
|
XM_011543675.1:c.11510T>G
|
XP_011541977.1:p.Leu3837Trp
|
|
XM_011543676.1:c.11432T>G
|
XP_011541978.1:p.Leu3811Trp
|
|
XM_011543677.1:c.8816T>G
|
XP_011541979.1:p.Leu2939Trp
|
|
XM_011543678.1:c.11513T>G
|
XP_011541980.1:p.Leu3838Trp
|
|
NM_032119.4:c.11513T>G
MANE Select
|
NP_115495.3:p.Leu3838Trp
|
|
XM_017009963.2:c.11534T>G
|
XP_016865452.1:p.Leu3845Trp
|
|
XM_017009964.2:c.11531T>G
|
XP_016865453.1:p.Leu3844Trp
|
|
XM_017009965.1:c.11531T>G
|
XP_016865454.1:p.Leu3844Trp
|
|
XM_017009966.2:c.11453T>G
|
XP_016865455.1:p.Leu3818Trp
|
|
XM_017009967.1:c.11438T>G
|
XP_016865456.1:p.Leu3813Trp
|
|
XM_017009968.2:c.11534T>G
|
XP_016865457.1:p.Leu3845Trp
|
|
XM_017009969.2:c.11534T>G
|
XP_016865458.1:p.Leu3845Trp
|
|
XM_017009970.2:c.11534T>G
|
XP_016865459.1:p.Leu3845Trp
|
|
XM_017009971.2:c.11534T>G
|
XP_016865460.1:p.Leu3845Trp
|
|
XM_017009972.1:c.4652T>G
|
XP_016865461.1:p.Leu1551Trp
|
|
XM_017009973.1:c.4631T>G
|
XP_016865462.1:p.Leu1544Trp
|
|
NR_003149.2:n.11529T>G
|
|
|