ENST00000435881.7:c.*2C>T
MANE Select
|
ENSP00000416627.1:n.*2C>T
|
|
ENST00000246912.8:c.*2C>T
|
ENSP00000246912.3:n.*2C>T
|
|
ENST00000346833.8:c.*2C>T
|
ENSP00000320913.3:n.*2C>T
|
|
ENST00000435881.6:c.*2C>T
|
ENSP00000416627.1:n.*2C>T
|
|
ENST00000585403.5:n.944C>T
|
|
|
ENST00000588320.1:n.1213C>T
|
|
|
ENST00000590050.5:n.903C>T
|
|
|
NM_170607.2:c.*2C>T
|
NP_733752.1:n.*2C>T
|
|
NM_198204.1:c.*2C>T
|
NP_937847.1:n.*2C>T
|
|
NM_198205.1:c.*2C>T
|
NP_937848.1:n.*2C>T
|
|
NM_198204.2:c.*2C>T
MANE Select
|
NP_937847.1:n.*2C>T
|
|
NM_170607.3:c.*2C>T
|
NP_733752.1:n.*2C>T
|
|
NM_198205.2:c.*2C>T
|
NP_937848.1:n.*2C>T
|
|