ENST00000377045.9:c.699+14G>C
MANE Select
|
ENSP00000366244.4:n.699+14G>C
|
|
ENST00000290277.10:c.708+14G>C
|
ENSP00000290277.7:n.708+14G>C
|
|
ENST00000377045.8:c.699+14G>C
|
ENSP00000366244.4:n.699+14G>C
|
|
NM_001256196.1:c.708+14G>C
|
NP_001243125.1:n.708+14G>C
|
|
NM_001654.4:c.699+14G>C
|
NP_001645.1:n.699+14G>C
|
|
XM_006724529.1:c.714+14G>C
|
XP_006724592.1:n.714+14G>C
|
|
XM_011543906.1:c.714+14G>C
|
XP_011542208.1:n.714+14G>C
|
|
XM_011543907.1:c.714+14G>C
|
XP_011542209.1:n.714+14G>C
|
|
XM_011543908.1:c.699+14G>C
|
XP_011542210.1:n.699+14G>C
|
|
XM_011543909.1:c.42+14G>C
|
XP_011542211.1:n.42+14G>C
|
|
XM_006724529.3:c.714+14G>C
|
XP_006724592.1:n.714+14G>C
|
|
XM_011543906.3:c.714+14G>C
|
XP_011542208.1:n.714+14G>C
|
|
XM_011543908.3:c.699+14G>C
|
XP_011542210.1:n.699+14G>C
|
|
XM_011543909.3:c.42+14G>C
|
XP_011542211.1:n.42+14G>C
|
|
NM_001654.5:c.699+14G>C
MANE Select
|
NP_001645.1:n.699+14G>C
|
|
NM_001256196.2:c.708+14G>C
|
NP_001243125.1:n.708+14G>C
|
|