ENST00000584483.6:n.2262G>T
|
|
|
ENST00000697953.1:n.2835G>T
|
|
|
ENST00000698013.1:n.2947G>T
|
|
|
ENST00000698014.1:n.3170G>T
|
|
|
ENST00000698015.1:n.2263G>T
|
|
|
ENST00000698016.1:c.*387G>T
|
ENSP00000513502.1:n.*387G>T
|
|
ENST00000698017.1:n.2337G>T
|
|
|
ENST00000698018.1:n.2468G>T
|
|
|
ENST00000698019.1:n.2666G>T
|
|
|
ENST00000698020.1:n.1772G>T
|
|
|
ENST00000698021.1:c.1681G>T
|
|
|
ENST00000698022.1:c.*387G>T
|
ENSP00000513504.1:n.*387G>T
|
|
ENST00000698023.1:n.2366G>T
|
|
|
ENST00000698024.1:n.2228G>T
|
|
|
ENST00000698025.1:n.2388G>T
|
|
|
ENST00000698026.1:n.1279G>T
|
|
|
ENST00000698027.1:c.*604G>T
|
ENSP00000513505.1:n.*604G>T
|
|
ENST00000698028.1:n.2471G>T
|
|
|
ENST00000698029.1:n.3200G>T
|
|
|
ENST00000448276.7:c.*387G>T
MANE Select
|
ENSP00000392617.2:n.*387G>T
|
|
ENST00000323347.14:c.*387G>T
|
ENSP00000318451.10:n.*387G>T
|
|
ENST00000448276.6:c.*387G>T
|
ENSP00000392617.2:n.*387G>T
|
|
ENST00000613943.4:c.1872G>T
|
ENSP00000483605.1:n.1872G>T
|
|
NM_001098426.1:c.*387G>T
|
NP_001091896.1:n.*387G>T
|
|
XM_005257604.2:c.*387G>T
|
XP_005257661.2:n.*387G>T
|
|
NM_001330439.1:c.*387G>T
|
NP_001317368.1:n.*387G>T
|
|
NM_001330440.1:c.*387G>T
|
NP_001317369.1:n.*387G>T
|
|
NM_001098426.2:c.*387G>T
MANE Select
|
NP_001091896.1:n.*387G>T
|
|
NM_001330440.2:c.*387G>T
|
NP_001317369.1:n.*387G>T
|
|