ENST00000367408.6:n.2924-193T>C
|
|
|
ENST00000367409.9:c.9637-193T>C
MANE Select
|
ENSP00000356379.4:n.9637-193T>C
|
|
ENST00000680265.1:c.9859-193T>C
|
ENSP00000505384.1:n.9859-193T>C
|
|
ENST00000680710.1:c.9613-193T>C
|
ENSP00000506676.1:n.9613-193T>C
|
|
ENST00000294732.11:c.4882-193T>C
|
ENSP00000294732.7:n.4882-193T>C
|
|
ENST00000367408.5:c.2632-193T>C
|
ENSP00000356378.1:n.2632-193T>C
|
|
ENST00000367409.8:c.9637-193T>C
|
ENSP00000356379.4:n.9637-193T>C
|
|
ENST00000612785.1:c.3595-193T>C
|
ENSP00000479244.1:n.3595-193T>C
|
|
NM_001206846.1:c.4882-193T>C
|
NP_001193775.1:n.4882-193T>C
|
|
NM_018136.4:c.9637-193T>C
|
NP_060606.3:n.9637-193T>C
|
|
NM_018136.5:c.9637-193T>C
MANE Select
|
NP_060606.3:n.9637-193T>C
|
|
NM_001206846.2:c.4882-193T>C
|
NP_001193775.1:n.4882-193T>C
|
|