ENST00000682565.1:c.10096G>C
|
ENSP00000507671.1:p.Asp3366His
|
|
ENST00000682801.1:c.10096G>C
|
ENSP00000507862.1:p.Asp3366His
|
|
ENST00000682859.1:c.10096G>C
|
ENSP00000508222.1:p.Asp3366His
|
|
ENST00000683791.1:c.3182G>C
|
|
|
ENST00000684460.1:c.7377G>C
|
|
|
ENST00000684548.1:c.10096G>C
|
ENSP00000507421.1:p.Asp3366His
|
|
ENST00000684590.1:c.4543G>C
|
ENSP00000507376.1:p.Asp1515His
|
|
ENST00000684656.1:c.7422G>C
|
|
|
ENST00000613296.6:c.10477G>C
MANE Select
|
ENSP00000482968.1:p.Asp3493His
|
|
ENST00000651057.1:c.631G>C
|
ENSP00000498504.1:p.Asp211His
|
|
ENST00000651434.1:c.1833G>C
|
|
|
ENST00000652487.1:c.1574G>C
|
|
|
ENST00000423048.5:c.3968G>C
|
ENSP00000399833.1:n.3968G>C
|
|
ENST00000484298.5:c.10351G>C
|
ENSP00000478155.1:p.Asp3451His
|
|
ENST00000613296.4:c.10477G>C
|
ENSP00000482968.1:p.Asp3493His
|
|
ENST00000614410.4:c.10477G>C
|
ENSP00000479094.1:p.Asp3493His
|
|
ENST00000620466.4:n.4280G>C
|
|
|
NM_015120.4:c.10480G>C , LRG_741t1:c.10480G>C
|
NP_055935.4:p.Asp3494His
|
|
NM_001378454.1:c.10477G>C
MANE Select
|
NP_001365383.1:p.Asp3493His
|
|