ENST00000252486.9:c.236+177T>C
MANE Select
|
ENSP00000252486.3:n.236+177T>C
|
|
ENST00000252486.8:c.236+177T>C
|
ENSP00000252486.3:n.236+177T>C
|
|
ENST00000425718.1:c.236+177T>C
|
ENSP00000410423.1:n.236+177T>C
|
|
ENST00000434152.5:c.314+177T>C
|
ENSP00000413653.2:n.314+177T>C
|
|
ENST00000446996.5:c.236+177T>C
|
ENSP00000413135.1:n.236+177T>C
|
|
NM_000041.3:c.236+177T>C
|
NP_000032.1:n.236+177T>C
|
|
NM_001302688.1:c.314+177T>C
|
NP_001289617.1:n.314+177T>C
|
|
NM_001302689.1:c.236+177T>C
|
NP_001289618.1:n.236+177T>C
|
|
NM_001302690.1:c.236+177T>C
|
NP_001289619.1:n.236+177T>C
|
|
NM_001302691.1:c.236+177T>C
|
NP_001289620.1:n.236+177T>C
|
|
NM_000041.4:c.236+177T>C
MANE Select
|
NP_000032.1:n.236+177T>C
|
|
NM_001302688.2:c.314+177T>C
|
NP_001289617.1:n.314+177T>C
|
|
NM_001302689.2:c.236+177T>C
|
NP_001289618.1:n.236+177T>C
|
|
NM_001302691.2:c.236+177T>C
|
NP_001289620.1:n.236+177T>C
|
|
NM_001302690.2:c.236+177T>C
|
NP_001289619.1:n.236+177T>C
|
|