ENST00000355773.6:c.881T>A
MANE Select
|
ENSP00000348019.5:p.Ile294Asn
|
|
ENST00000355773.5:c.881T>A
|
ENSP00000348019.5:p.Ile294Asn
|
|
NM_012434.4:c.881T>A
|
NP_036566.1:p.Ile294Asn
|
|
XM_005248710.2:c.830T>A
|
XP_005248767.1:p.Ile277Asn
|
|
XM_005248711.1:c.683T>A
|
XP_005248768.1:p.Ile228Asn
|
|
XM_011535750.1:c.881T>A
|
XP_011534052.1:p.Ile294Asn
|
|
NM_012434.5:c.881T>A
MANE Select
|
NP_036566.1:p.Ile294Asn
|
|
NM_001382629.1:c.650T>A
|
NP_001369558.1:p.Ile217Asn
|
|
NM_001382630.1:c.881T>A
|
NP_001369559.1:p.Ile294Asn
|
|
NM_001382631.1:c.902T>A
|
NP_001369560.1:p.Ile301Asn
|
|
NM_001382632.1:c.794T>A
|
NP_001369561.1:p.Ile265Asn
|
|
NM_001382633.1:c.881T>A
|
NP_001369562.1:p.Ile294Asn
|
|
NM_001382634.1:c.820-6454T>A
|
NP_001369563.1:n.820-6454T>A
|
|
NM_001382635.1:c.878T>A
|
NP_001369564.1:p.Ile293Asn
|
|
NM_001382636.1:c.563T>A
|
NP_001369565.1:p.Ile188Asn
|
|