ENST00000682565.1:c.11699A>C
|
ENSP00000507671.1:p.Asp3900Ala
|
|
ENST00000682801.1:c.11167-783A>C
|
ENSP00000507862.1:n.11167-783A>C
|
|
ENST00000682859.1:c.11699A>C
|
ENSP00000508222.1:p.Asp3900Ala
|
|
ENST00000683791.1:c.4785A>C
|
|
|
ENST00000684460.1:c.8980A>C
|
|
|
ENST00000684548.1:c.11699A>C
|
ENSP00000507421.1:p.Asp3900Ala
|
|
ENST00000684590.1:c.6146A>C
|
ENSP00000507376.1:p.Asp2049Ala
|
|
ENST00000684656.1:c.9164A>C
|
|
|
ENST00000613296.6:c.12080A>C
MANE Select
|
ENSP00000482968.1:p.Asp4027Ala
|
|
ENST00000651057.1:c.2234A>C
|
ENSP00000498504.1:p.Asp745Ala
|
|
ENST00000651434.1:c.3436A>C
|
|
|
ENST00000651750.1:c.1260+521A>C
|
|
|
ENST00000652487.1:c.3251A>C
|
|
|
ENST00000464408.3:n.255A>C
|
|
|
ENST00000484298.5:c.11954A>C
|
ENSP00000478155.1:p.Asp3985Ala
|
|
ENST00000613296.4:c.12080A>C
|
ENSP00000482968.1:p.Asp4027Ala
|
|
ENST00000620466.4:n.5883A>C
|
|
|
NM_015120.4:c.12083A>C , LRG_741t1:c.12083A>C
|
NP_055935.4:p.Asp4028Ala
|
|
NM_001378454.1:c.12080A>C
MANE Select
|
NP_001365383.1:p.Asp4027Ala
|
|