ENST00000470094.2:c.*347G>T
|
ENSP00000434898.2:n.*347G>T
|
|
ENST00000528762.2:c.*1191G>T
|
ENSP00000433168.2:n.*1191G>T
|
|
ENST00000530893.7:c.9455G>T
|
ENSP00000499438.2:p.Ser3152Ile
|
|
ENST00000665585.2:c.*1386G>T
|
ENSP00000499570.2:n.*1386G>T
|
|
ENST00000700202.2:c.9773G>T
|
ENSP00000514856.2:p.Ser3258Ile
|
|
ENST00000700202.1:c.2240G>T
|
ENSP00000514856.1:p.Ser747Ile
|
|
ENST00000700203.1:n.1951G>T
|
|
|
ENST00000380152.8:c.9824G>T
MANE Select
|
ENSP00000369497.3:p.Ser3275Ile
|
|
ENST00000544455.6:c.9824G>T
|
ENSP00000439902.1:p.Ser3275Ile
|
|
ENST00000614259.2:c.9832G>T
|
ENSP00000506251.1:n.9832G>T
|
|
ENST00000680887.1:c.9824G>T
|
ENSP00000505508.1:p.Ser3275Ile
|
|
ENST00000380152.7:c.9824G>T
|
ENSP00000369497.3:p.Ser3275Ile
|
|
ENST00000533776.1:n.412G>T
|
|
|
ENST00000544455.5:c.9824G>T
|
ENSP00000439902.1:p.Ser3275Ile
|
|
NM_000059.3:c.9824G>T , LRG_293t1:c.9824G>T
|
NP_000050.2:p.Ser3275Ile
|
|
XM_011535203.1:c.9824G>T
|
XP_011533505.1:p.Ser3275Ile
|
|
XM_011535204.1:c.9728G>T
|
XP_011533506.1:p.Ser3243Ile
|
|
NM_000059.4:c.9824G>T
MANE Select
|
NP_000050.3:p.Ser3275Ile
|
|