ENST00000253788.12:c.81+360A>C
MANE Select
|
ENSP00000253788.5:n.81+360A>C
|
|
ENST00000589913.6:c.81+360A>C
|
ENSP00000464813.1:n.81+360A>C
|
|
ENST00000590864.2:c.87A>C
|
ENSP00000467939.2:p.Gly29=
|
|
ENST00000253788.9:c.81+360A>C
|
ENSP00000253788.4:n.81+360A>C
|
|
ENST00000586277.5:c.104+279A>C
|
|
|
ENST00000587478.1:n.496A>C
|
|
|
ENST00000588830.1:c.81+360A>C
|
ENSP00000468468.1:n.81+360A>C
|
|
ENST00000589037.5:c.81+360A>C
|
ENSP00000467587.1:n.81+360A>C
|
|
ENST00000589913.5:c.81+360A>C
|
ENSP00000464813.1:n.81+360A>C
|
|
ENST00000593262.1:n.773A>C
|
|
|
NM_000988.3:c.81+360A>C
|
NP_000979.1:n.81+360A>C
|
|
NM_000988.5:c.81+360A>C
MANE Select
|
NP_000979.1:n.81+360A>C
|
|
NM_001349921.1:c.81+360A>C
|
NP_001336850.1:n.81+360A>C
|
|
NM_001349922.1:c.81+360A>C
|
NP_001336851.1:n.81+360A>C
|
|
NR_146327.1:n.164+360A>C
|
|
|
NM_001349921.2:c.81+360A>C
|
NP_001336850.1:n.81+360A>C
|
|
NM_001349922.2:c.81+360A>C
|
NP_001336851.1:n.81+360A>C
|
|
NR_146327.2:n.136+360A>C
|
|
|