ENST00000682565.1:c.11505T>G
|
ENSP00000507671.1:p.Phe3835Leu
|
|
ENST00000682801.1:c.11167-977T>G
|
ENSP00000507862.1:n.11167-977T>G
|
|
ENST00000682859.1:c.11505T>G
|
ENSP00000508222.1:p.Phe3835Leu
|
|
ENST00000683791.1:c.4591T>G
|
|
|
ENST00000684460.1:c.8786T>G
|
|
|
ENST00000684548.1:c.11505T>G
|
ENSP00000507421.1:p.Phe3835Leu
|
|
ENST00000684590.1:c.5952T>G
|
ENSP00000507376.1:p.Phe1984Leu
|
|
ENST00000684656.1:c.8970T>G
|
|
|
ENST00000613296.6:c.11886T>G
MANE Select
|
ENSP00000482968.1:p.Phe3962Leu
|
|
ENST00000651057.1:c.2040T>G
|
ENSP00000498504.1:p.Phe680Leu
|
|
ENST00000651434.1:c.3242T>G
|
|
|
ENST00000651750.1:c.1260+327T>G
|
|
|
ENST00000652487.1:c.3057T>G
|
|
|
ENST00000464408.3:n.61T>G
|
|
|
ENST00000484298.5:c.11760T>G
|
ENSP00000478155.1:p.Phe3920Leu
|
|
ENST00000613296.4:c.11886T>G
|
ENSP00000482968.1:p.Phe3962Leu
|
|
ENST00000620466.4:n.5689T>G
|
|
|
NM_015120.4:c.11889T>G , LRG_741t1:c.11889T>G
|
NP_055935.4:p.Phe3963Leu
|
|
NM_001378454.1:c.11886T>G
MANE Select
|
NP_001365383.1:p.Phe3962Leu
|
|