ENST00000348729.8:c.782T>C
MANE Select
|
ENSP00000302701.4:p.Ile261Thr
|
|
ENST00000348729.7:c.782T>C
|
ENSP00000302701.4:p.Ile261Thr
|
|
ENST00000353963.7:c.794T>C
|
ENSP00000302851.5:p.Ile265Thr
|
|
ENST00000504513.1:c.164+135T>C
|
|
|
ENST00000506512.1:n.393T>C
|
|
|
NM_005847.4:c.782T>C
|
NP_005838.3:p.Ile261Thr
|
|
NM_152685.3:c.794T>C
|
NP_689898.2:p.Ile265Thr
|
|
XM_005272148.3:c.902T>C
|
XP_005272205.3:p.Ile301Thr
|
|
XM_005272149.3:c.890T>C
|
XP_005272206.3:p.Ile297Thr
|
|
XM_006714741.2:c.902T>C
|
XP_006714804.2:p.Ile301Thr
|
|
XM_011543765.1:c.902T>C
|
XP_011542067.1:p.Ile301Thr
|
|
XM_011543766.1:c.683T>C
|
XP_011542068.1:p.Ile228Thr
|
|
XM_011543767.1:c.587T>C
|
XP_011542069.1:p.Ile196Thr
|
|
XM_011543768.1:c.467T>C
|
XP_011542070.1:p.Ile156Thr
|
|
XM_011543769.1:c.77T>C
|
XP_011542071.1:p.Ile26Thr
|
|
XM_005272149.4:c.890T>C
|
XP_005272206.3:p.Ile297Thr
|
|
XM_011543765.2:c.902T>C
|
XP_011542067.1:p.Ile301Thr
|
|
NM_005847.5:c.782T>C
MANE Select
|
NP_005838.3:p.Ile261Thr
|
|
NM_152685.4:c.794T>C
|
NP_689898.2:p.Ile265Thr
|
|