ENST00000697602.1:n.1031+2T>C
|
|
|
ENST00000697603.1:c.3135+2T>C
|
ENSP00000513358.1:n.3135+2T>C
|
|
ENST00000314191.7:c.10458+2T>C
MANE Select
|
ENSP00000313420.3:n.10458+2T>C
|
|
ENST00000314191.6:c.10458+2T>C
|
ENSP00000313420.3:n.10458+2T>C
|
|
ENST00000338368.7:c.10458+2T>C
|
ENSP00000345182.4:n.10458+2T>C
|
|
NM_001081640.1:c.10458+2T>C
|
NP_001075109.1:n.10458+2T>C
|
|
NM_006904.6:c.10458+2T>C , LRG_162t1:c.10458+2T>C
|
NP_008835.5:n.10458+2T>C
|
|
XM_011517567.1:c.10461+2T>C
|
XP_011515869.1:n.10461+2T>C
|
|
XM_011517568.1:c.10461+2T>C
|
XP_011515870.1:n.10461+2T>C
|
|
NM_001081640.2:c.10458+2T>C
|
NP_001075109.1:n.10458+2T>C
|
|
NM_006904.7:c.10458+2T>C
MANE Select
|
NP_008835.5:n.10458+2T>C
|
|