ENST00000367408.6:n.3336T>G
|
|
|
ENST00000367409.9:c.10049T>G
MANE Select
|
ENSP00000356379.4:p.Leu3350Trp
|
|
ENST00000680265.1:c.10271T>G
|
ENSP00000505384.1:p.Leu3424Trp
|
|
ENST00000680710.1:c.10025T>G
|
ENSP00000506676.1:p.Leu3342Trp
|
|
ENST00000294732.11:c.5294T>G
|
ENSP00000294732.7:p.Leu1765Trp
|
|
ENST00000367408.5:c.3044T>G
|
ENSP00000356378.1:p.Leu1015Trp
|
|
ENST00000367409.8:c.10049T>G
|
ENSP00000356379.4:p.Leu3350Trp
|
|
ENST00000612785.1:c.4007T>G
|
ENSP00000479244.1:p.Leu1336Trp
|
|
NM_001206846.1:c.5294T>G
|
NP_001193775.1:p.Leu1765Trp
|
|
NM_018136.4:c.10049T>G
|
NP_060606.3:p.Leu3350Trp
|
|
NM_018136.5:c.10049T>G
MANE Select
|
NP_060606.3:p.Leu3350Trp
|
|
NM_001206846.2:c.5294T>G
|
NP_001193775.1:p.Leu1765Trp
|
|