ENST00000378623.6:c.3256A>G
MANE Select
|
ENSP00000367888.1:p.Ile1086Val
|
|
ENST00000378623.5:c.3256A>G
|
ENSP00000367888.1:p.Ile1086Val
|
|
NM_002334.3:c.3256A>G
|
NP_002325.2:p.Ile1086Val
|
|
XM_011520102.1:c.3469A>G
|
XP_011518404.1:p.Ile1157Val
|
|
XM_011520103.1:c.2452A>G
|
XP_011518405.1:p.Ile818Val
|
|
XM_011520104.1:c.1021A>G
|
XP_011518406.1:p.Ile341Val
|
|
XM_011520103.2:c.2452A>G
|
XP_011518405.1:p.Ile818Val
|
|
XM_011520104.2:c.1021A>G
|
XP_011518406.1:p.Ile341Val
|
|
XM_017017734.1:c.3256A>G
|
XP_016873223.1:p.Ile1086Val
|
|
NM_002334.4:c.3256A>G
MANE Select
|
NP_002325.2:p.Ile1086Val
|
|