ENST00000403665.7:c.1353A>C
MANE Select
|
ENSP00000384957.2:p.Gln451His
|
|
ENST00000264691.4:c.49A>C
|
|
|
ENST00000264692.8:c.1191A>C
|
ENSP00000264692.5:p.Gln397His
|
|
ENST00000403665.6:c.1353A>C
|
ENSP00000384957.2:p.Gln451His
|
|
NM_000128.3:c.1353A>C , LRG_583t1:c.1353A>C
|
NP_000119.1:p.Gln451His
|
|
XM_005262821.2:c.1356A>C
|
XP_005262878.1:p.Gln452His
|
|
XM_005262822.2:c.1356A>C
|
XP_005262879.1:p.Gln452His
|
|
XM_005262823.2:c.1086A>C
|
XP_005262880.1:p.Gln362His
|
|
XM_005262824.1:c.1356A>C
|
XP_005262881.1:p.Gln452His
|
|
XM_006714137.1:c.1308A>C
|
XP_006714200.1:p.Gln436His
|
|
XR_938706.1:n.1761A>C
|
|
|
XR_938707.1:n.1761A>C
|
|
|
XM_005262821.4:c.1356A>C
|
XP_005262878.1:p.Gln452His
|
|
XM_005262822.4:c.1356A>C
|
XP_005262879.1:p.Gln452His
|
|
XM_005262823.4:c.1086A>C
|
XP_005262880.1:p.Gln362His
|
|
XM_006714137.3:c.1308A>C
|
XP_006714200.1:p.Gln436His
|
|
XR_001741172.2:n.1827A>C
|
|
|
NM_000128.4:c.1353A>C
MANE Select
|
NP_000119.1:p.Gln451His
|
|