|
NM_005744.5:c.912-16T>C
MANE Select
|
NP_005735.2:n.912-16T>C
|
|
ENST00000379887.9:c.912-16T>C
MANE Select
|
ENSP00000369217.4:n.912-16T>C
|
|
NM_005744.3:c.912-16T>C
|
NP_005735.2:n.912-16T>C
|
|
NM_005744.4:c.912-16T>C
|
NP_005735.2:n.912-16T>C
|
|
ENST00000379887.8:c.912-16T>C
|
ENSP00000369217.4:n.912-16T>C
|
|
ENST00000561987.5:n.98+4998T>C
|
|
|
ENST00000565950.1:n.178T>C
|
|
|
XM_011521438.1:c.735-16T>C
|
XP_011519740.1:n.735-16T>C
|
|
XM_011521438.3:c.735-16T>C
|
XP_011519740.1:n.735-16T>C
|
|
XM_011521439.1:c.636-16T>C
|
XP_011519741.1:n.636-16T>C
|
|
XM_011521439.3:c.636-16T>C
|
XP_011519741.1:n.636-16T>C
|