ENST00000374580.10:c.418+25T>C
MANE Select
|
ENSP00000363708.4:n.418+25T>C
|
|
ENST00000638587.1:c.349+25T>C
|
ENSP00000491062.1:n.349+25T>C
|
|
ENST00000374574.2:c.418+25T>C
|
ENSP00000363702.2:n.418+25T>C
|
|
ENST00000374580.8:c.418+25T>C
|
ENSP00000363708.4:n.418+25T>C
|
|
ENST00000479069.1:n.325+25T>C
|
|
|
NM_001204.6:c.418+25T>C , LRG_712t1:c.418+25T>C
|
NP_001195.2:n.418+25T>C
|
|
XM_011511687.1:c.418+25T>C
|
XP_011509989.1:n.418+25T>C
|
|
XM_011511688.1:c.418+25T>C
|
XP_011509990.1:n.418+25T>C
|
|
NM_001204.7:c.418+25T>C
MANE Select
|
NP_001195.2:n.418+25T>C
|
|