ENST00000265104.5:c.9143T>C
MANE Select
|
ENSP00000265104.4:p.Ile3048Thr
|
|
ENST00000681290.1:c.9098T>C
|
ENSP00000505288.1:p.Ile3033Thr
|
|
ENST00000265104.4:c.9143T>C
|
ENSP00000265104.4:p.Ile3048Thr
|
|
NM_001369.2:c.9143T>C
|
NP_001360.1:p.Ile3048Thr
|
|
XM_005248262.2:c.9098T>C
|
XP_005248319.1:p.Ile3033Thr
|
|
XM_011513990.1:c.*30T>C
|
XP_011512292.1:n.*30T>C
|
|
XR_925598.1:n.9214T>C
|
|
|
XM_005248262.3:c.9251T>C
|
XP_005248319.2:p.Ile3084Thr
|
|
XM_017009177.1:c.9251T>C
|
XP_016864666.1:p.Ile3084Thr
|
|
XM_017009178.1:c.8156T>C
|
XP_016864667.1:p.Ile2719Thr
|
|
XM_017009179.2:c.8156T>C
|
XP_016864668.1:p.Ile2719Thr
|
|
XM_017009180.1:c.9251T>C
|
XP_016864669.1:p.Ile3084Thr
|
|
XM_017009181.1:c.9251T>C
|
XP_016864670.1:p.Ile3084Thr
|
|
XM_017009182.1:c.9251T>C
|
XP_016864671.1:p.Ile3084Thr
|
|
XM_017009183.1:c.9251T>C
|
XP_016864672.1:p.Ile3084Thr
|
|
XM_017009184.1:c.*30T>C
|
XP_016864673.1:n.*30T>C
|
|
XM_017009185.1:c.4340T>C
|
XP_016864674.1:p.Ile1447Thr
|
|
XM_017009186.1:c.3893T>C
|
XP_016864675.1:p.Ile1298Thr
|
|
XM_017009188.1:c.3230T>C
|
XP_016864677.1:p.Ile1077Thr
|
|
XM_024454388.1:c.8156T>C
|
XP_024310156.1:p.Ile2719Thr
|
|
XM_024454389.1:c.7745T>C
|
XP_024310157.1:p.Ile2582Thr
|
|
XR_001742034.1:n.9137T>C
|
|
|
XR_001742035.1:n.9132T>C
|
|
|
NM_001369.3:c.9143T>C
MANE Select
|
NP_001360.1:p.Ile3048Thr
|
|