ENST00000241416.12:c.55+9657A>G
MANE Select
|
ENSP00000241416.7:n.55+9657A>G
|
|
ENST00000241416.11:c.55+9657A>G
|
ENSP00000241416.7:n.55+9657A>G
|
|
ENST00000404590.1:c.55+9657A>G
|
ENSP00000384338.1:n.55+9657A>G
|
|
ENST00000462659.1:n.183+10158A>G
|
|
|
ENST00000465329.1:n.179+9657A>G
|
|
|
ENST00000487959.5:n.190+10158A>G
|
|
|
ENST00000535787.5:c.-207+10158A>G
|
ENSP00000439988.1:n.-207+10158A>G
|
|
NM_001278579.1:c.55+9657A>G
|
NP_001265508.1:n.55+9657A>G
|
|
NM_001278580.1:c.-207+10158A>G
|
NP_001265509.1:n.-207+10158A>G
|
|
NM_001616.4:c.55+9657A>G
|
NP_001607.1:n.55+9657A>G
|
|
XM_005263843.2:c.55+9657A>G
|
XP_005263900.1:n.55+9657A>G
|
|
NM_001616.5:c.55+9657A>G
MANE Select
|
NP_001607.1:n.55+9657A>G
|
|
NM_001278579.2:c.55+9657A>G
|
NP_001265508.1:n.55+9657A>G
|
|
NM_001278580.2:c.-207+10158A>G
|
NP_001265509.1:n.-207+10158A>G
|
|