ENST00000373631.8:c.3776G>T
MANE Select
|
ENSP00000362734.3:p.Ser1259Ile
|
|
ENST00000373631.7:c.3776G>T
|
ENSP00000362734.3:p.Ser1259Ile
|
|
ENST00000460253.1:c.2780G>T
|
ENSP00000435279.1:p.Ser927Ile
|
|
NM_173689.6:c.3776G>T
|
NP_775960.4:p.Ser1259Ile
|
|
NR_104603.1:n.2890G>T
|
|
|
XM_005251934.1:c.2780G>T
|
XP_005251991.1:p.Ser927Ile
|
|
XM_011518556.1:c.3749G>T
|
XP_011516858.1:p.Ser1250Ile
|
|
XM_011518557.1:c.3581G>T
|
XP_011516859.1:p.Ser1194Ile
|
|
XM_011518558.1:c.3581G>T
|
XP_011516860.1:p.Ser1194Ile
|
|
XM_005251934.3:c.2780G>T
|
XP_005251991.1:p.Ser927Ile
|
|
XM_011518556.3:c.3749G>T
|
XP_011516858.1:p.Ser1250Ile
|
|
XM_011518557.3:c.3581G>T
|
XP_011516859.1:p.Ser1194Ile
|
|
XM_011518558.3:c.3581G>T
|
XP_011516860.1:p.Ser1194Ile
|
|
NM_173689.7:c.3776G>T
MANE Select
|
NP_775960.4:p.Ser1259Ile
|
|
NR_104603.2:n.2890G>T
|
|
|