ENST00000470094.2:c.*267G>T
|
ENSP00000434898.2:n.*267G>T
|
|
ENST00000528762.2:c.*1111G>T
|
ENSP00000433168.2:n.*1111G>T
|
|
ENST00000530893.7:c.9375G>T
|
ENSP00000499438.2:p.Met3125Ile
|
|
ENST00000665585.2:c.*1306G>T
|
ENSP00000499570.2:n.*1306G>T
|
|
ENST00000700202.2:c.9693G>T
|
ENSP00000514856.2:p.Met3231Ile
|
|
ENST00000700202.1:c.2160G>T
|
ENSP00000514856.1:p.Met720Ile
|
|
ENST00000700203.1:n.1871G>T
|
|
|
ENST00000380152.8:c.9744G>T
MANE Select
|
ENSP00000369497.3:p.Met3248Ile
|
|
ENST00000544455.6:c.9744G>T
|
ENSP00000439902.1:p.Met3248Ile
|
|
ENST00000614259.2:c.9752G>T
|
ENSP00000506251.1:n.9752G>T
|
|
ENST00000680887.1:c.9744G>T
|
ENSP00000505508.1:p.Met3248Ile
|
|
ENST00000380152.7:c.9744G>T
|
ENSP00000369497.3:p.Met3248Ile
|
|
ENST00000470094.1:c.827G>T
|
|
|
ENST00000533776.1:n.332G>T
|
|
|
ENST00000544455.5:c.9744G>T
|
ENSP00000439902.1:p.Met3248Ile
|
|
NM_000059.3:c.9744G>T , LRG_293t1:c.9744G>T
|
NP_000050.2:p.Met3248Ile
|
|
XM_011535203.1:c.9744G>T
|
XP_011533505.1:p.Met3248Ile
|
|
XM_011535204.1:c.9648G>T
|
XP_011533506.1:p.Met3216Ile
|
|
NM_000059.4:c.9744G>T
MANE Select
|
NP_000050.3:p.Met3248Ile
|
|