ENST00000682565.1:c.7415G>A
|
ENSP00000507671.1:p.Arg2472Lys
|
|
ENST00000682801.1:c.7415G>A
|
ENSP00000507862.1:p.Arg2472Lys
|
|
ENST00000682859.1:c.7415G>A
|
ENSP00000508222.1:p.Arg2472Lys
|
|
ENST00000683791.1:c.807G>A
|
|
|
ENST00000684460.1:c.4867G>A
|
|
|
ENST00000684548.1:c.7415G>A
|
ENSP00000507421.1:p.Arg2472Lys
|
|
ENST00000684590.1:c.1862G>A
|
ENSP00000507376.1:p.Arg621Lys
|
|
ENST00000684656.1:c.4867G>A
|
|
|
ENST00000613296.6:c.7796G>A
MANE Select
|
ENSP00000482968.1:p.Arg2599Lys
|
|
ENST00000651434.1:c.896-30020G>A
|
|
|
ENST00000423048.5:c.2627G>A
|
ENSP00000399833.1:p.Arg876Lys
|
|
ENST00000484298.5:c.7670G>A
|
ENSP00000478155.1:p.Arg2557Lys
|
|
ENST00000613296.4:c.7796G>A
|
ENSP00000482968.1:p.Arg2599Lys
|
|
ENST00000614410.4:c.7796G>A
|
ENSP00000479094.1:p.Arg2599Lys
|
|
ENST00000620466.4:n.1599G>A
|
|
|
NM_015120.4:c.7799G>A , LRG_741t1:c.7799G>A
|
NP_055935.4:p.Arg2600Lys
|
|
NM_001378454.1:c.7796G>A
MANE Select
|
NP_001365383.1:p.Arg2599Lys
|
|