ENST00000355773.6:c.1264G>C
MANE Select
|
ENSP00000348019.5:p.Ala422Pro
|
|
ENST00000355773.5:c.1264G>C
|
ENSP00000348019.5:p.Ala422Pro
|
|
NM_012434.4:c.1264G>C
|
NP_036566.1:p.Ala422Pro
|
|
XM_005248710.2:c.1213G>C
|
XP_005248767.1:p.Ala405Pro
|
|
XM_005248711.1:c.1066G>C
|
XP_005248768.1:p.Ala356Pro
|
|
XM_011535750.1:c.1116G>C
|
XP_011534052.1:p.Met372Ile
|
|
NM_012434.5:c.1264G>C
MANE Select
|
NP_036566.1:p.Ala422Pro
|
|
NM_001382629.1:c.1033G>C
|
NP_001369558.1:p.Ala345Pro
|
|
NM_001382630.1:c.1260-5223G>C
|
NP_001369559.1:n.1260-5223G>C
|
|
NM_001382631.1:c.1285G>C
|
NP_001369560.1:p.Ala429Pro
|
|
NM_001382632.1:c.1177G>C
|
NP_001369561.1:p.Ala393Pro
|
|
NM_001382633.1:c.1264G>C
|
NP_001369562.1:p.Ala422Pro
|
|
NM_001382634.1:c.1105G>C
|
NP_001369563.1:p.Ala369Pro
|
|
NM_001382635.1:c.1261G>C
|
NP_001369564.1:p.Ala421Pro
|
|
NM_001382636.1:c.946G>C
|
NP_001369565.1:p.Ala316Pro
|
|