ENST00000355773.6:c.1306C>T
MANE Select
|
ENSP00000348019.5:p.Pro436Ser
|
|
ENST00000355773.5:c.1306C>T
|
ENSP00000348019.5:p.Pro436Ser
|
|
NM_012434.4:c.1306C>T
|
NP_036566.1:p.Pro436Ser
|
|
XM_005248710.2:c.1255C>T
|
XP_005248767.1:p.Pro419Ser
|
|
XM_005248711.1:c.1108C>T
|
XP_005248768.1:p.Pro370Ser
|
|
XM_011535750.1:c.1158C>T
|
XP_011534052.1:p.Phe386=
|
|
NM_012434.5:c.1306C>T
MANE Select
|
NP_036566.1:p.Pro436Ser
|
|
NM_001382629.1:c.1075C>T
|
NP_001369558.1:p.Pro359Ser
|
|
NM_001382630.1:c.1260-5181C>T
|
NP_001369559.1:n.1260-5181C>T
|
|
NM_001382631.1:c.1327C>T
|
NP_001369560.1:p.Pro443Ser
|
|
NM_001382632.1:c.1219C>T
|
NP_001369561.1:p.Pro407Ser
|
|
NM_001382633.1:c.1306C>T
|
NP_001369562.1:p.Pro436Ser
|
|
NM_001382634.1:c.1147C>T
|
NP_001369563.1:p.Pro383Ser
|
|
NM_001382635.1:c.1303C>T
|
NP_001369564.1:p.Pro435Ser
|
|
NM_001382636.1:c.988C>T
|
NP_001369565.1:p.Pro330Ser
|
|