ENST00000327047.6:c.355T>C
MANE Select
|
ENSP00000322280.1:p.Phe119Leu
|
|
ENST00000468836.2:c.503T>C
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ENSP00000419892.2:p.Leu168Pro
|
|
ENST00000644099.1:c.347T>C
|
ENSP00000494762.1:n.347T>C
|
|
ENST00000295911.6:c.127T>C
|
ENSP00000295911.2:p.Phe43Leu
|
|
ENST00000327047.5:c.355T>C
|
ENSP00000322280.1:p.Phe119Leu
|
|
ENST00000328863.8:c.355T>C
|
ENSP00000329158.4:p.Phe119Leu
|
|
ENST00000468836.1:c.127T>C
|
ENSP00000419892.1:p.Phe43Leu
|
|
ENST00000472224.1:n.361T>C
|
|
|
ENST00000485607.1:c.19T>C
|
ENSP00000419244.1:p.Phe7Leu
|
|
ENST00000562308.5:c.26T>C
|
|
|
ENST00000565169.1:c.84T>C
|
|
|
ENST00000569170.5:c.84T>C
|
|
|
NM_001195794.1:c.355T>C , LRG_700t1:c.355T>C
|
NP_001182723.1:p.Phe119Leu
|
|
NM_001256819.1:c.527T>C
|
NP_001243748.1:p.Leu176Pro
|
|
NM_052995.2:c.127T>C , LRG_700t2:c.127T>C
|
NP_443721.1:p.Phe43Leu
|
|
NM_174878.2:c.355T>C
|
NP_777367.1:p.Phe119Leu
|
|
NR_046380.2:n.797T>C
|
|
|
XR_924167.1:n.667T>C
|
|
|
NM_001256819.2:c.527T>C
|
NP_001243748.1:p.Leu176Pro
|
|
NM_174878.3:c.355T>C
MANE Select
|
NP_777367.1:p.Phe119Leu
|
|
NR_046380.3:n.525T>C
|
|
|