ENST00000318407.5:c.349+1065C>T
MANE Select
|
ENSP00000314132.3:n.349+1065C>T
|
|
ENST00000318407.4:c.349+1065C>T
|
ENSP00000314132.3:n.349+1065C>T
|
|
NM_032515.4:c.349+1065C>T
|
NP_115904.1:n.349+1065C>T
|
|
XM_005247037.3:c.349+1065C>T
|
XP_005247094.1:n.349+1065C>T
|
|
XM_005247039.3:c.115+1065C>T
|
XP_005247096.1:n.115+1065C>T
|
|
XM_011511696.1:c.349+1065C>T
|
XP_011509998.1:n.349+1065C>T
|
|
XM_011511697.1:c.349+1065C>T
|
XP_011509999.1:n.349+1065C>T
|
|
XM_011511696.2:c.349+1065C>T
|
XP_011509998.1:n.349+1065C>T
|
|
XM_011511697.3:c.349+1065C>T
|
XP_011509999.1:n.349+1065C>T
|
|
XM_017004775.1:c.115+1065C>T
|
XP_016860264.1:n.115+1065C>T
|
|
XM_017004776.1:c.115+1065C>T
|
XP_016860265.1:n.115+1065C>T
|
|
NM_032515.5:c.349+1065C>T
MANE Select
|
NP_115904.1:n.349+1065C>T
|
|