ENST00000682565.1:c.7802A>T
|
ENSP00000507671.1:p.Asn2601Ile
|
|
ENST00000682801.1:c.7802A>T
|
ENSP00000507862.1:p.Asn2601Ile
|
|
ENST00000682859.1:c.7802A>T
|
ENSP00000508222.1:p.Asn2601Ile
|
|
ENST00000683791.1:c.1194A>T
|
|
|
ENST00000684460.1:c.5254A>T
|
|
|
ENST00000684548.1:c.7802A>T
|
ENSP00000507421.1:p.Asn2601Ile
|
|
ENST00000684590.1:c.2249A>T
|
ENSP00000507376.1:p.Asn750Ile
|
|
ENST00000684656.1:c.5254A>T
|
|
|
ENST00000613296.6:c.8183A>T
MANE Select
|
ENSP00000482968.1:p.Asn2728Ile
|
|
ENST00000651434.1:c.896-29633A>T
|
|
|
ENST00000423048.5:c.3014A>T
|
ENSP00000399833.1:p.Asn1005Ile
|
|
ENST00000484298.5:c.8057A>T
|
ENSP00000478155.1:p.Asn2686Ile
|
|
ENST00000613296.4:c.8183A>T
|
ENSP00000482968.1:p.Asn2728Ile
|
|
ENST00000614410.4:c.8183A>T
|
ENSP00000479094.1:p.Asn2728Ile
|
|
ENST00000620466.4:n.1986A>T
|
|
|
NM_015120.4:c.8186A>T , LRG_741t1:c.8186A>T
|
NP_055935.4:p.Asn2729Ile
|
|
NM_001378454.1:c.8183A>T
MANE Select
|
NP_001365383.1:p.Asn2728Ile
|
|