ENST00000652197.2:c.-76+3884C>T
|
ENSP00000498301.2:n.-76+3884C>T
|
|
ENST00000402280.6:c.2-212C>T
MANE Select
|
ENSP00000385428.1:n.2-212C>T
|
|
ENST00000404025.3:c.2-212C>T
|
ENSP00000385090.3:n.2-212C>T
|
|
ENST00000652197.1:c.2-212C>T
|
ENSP00000498301.1:n.2-212C>T
|
|
ENST00000342905.10:c.2-212C>T
|
ENSP00000339666.6:n.2-212C>T
|
|
ENST00000360906.9:c.2-212C>T
|
ENSP00000354159.5:n.2-212C>T
|
|
ENST00000402280.5:c.2-212C>T
|
ENSP00000385428.1:n.2-212C>T
|
|
ENST00000404025.2:c.2-212C>T
|
ENSP00000385090.2:n.2-212C>T
|
|
NM_001199138.1:c.2-212C>T
|
NP_001186067.1:n.2-212C>T
|
|
NM_001199139.1:c.2-212C>T
|
NP_001186068.1:n.2-212C>T
|
|
NM_001302504.1:c.2-212C>T
|
NP_001289433.1:n.2-212C>T
|
|
NM_021209.4:c.2-212C>T
|
NP_067032.3:n.2-212C>T
|
|
XM_011533008.1:c.2-212C>T
|
XP_011531310.1:n.2-212C>T
|
|
XM_017004619.1:c.2-212C>T
|
XP_016860108.1:n.2-212C>T
|
|
XR_001738872.1:n.263-212C>T
|
|
|
NM_001199138.2:c.2-212C>T
MANE Select
|
NP_001186067.1:n.2-212C>T
|
|