ENST00000373290.7:c.357+677T>G
MANE Select
|
ENSP00000362387.2:n.357+677T>G
|
|
ENST00000373290.6:c.357+677T>G
|
ENSP00000362387.2:n.357+677T>G
|
|
ENST00000452130.1:c.84+677T>G
|
ENSP00000404528.1:n.84+677T>G
|
|
ENST00000475069.5:n.127+677T>G
|
|
|
NM_012339.3:c.357+677T>G
|
NP_036471.1:n.357+677T>G
|
|
XM_005269667.3:c.97-9702T>G
|
XP_005269724.1:n.97-9702T>G
|
|
XM_006717738.2:c.285+677T>G
|
XP_006717801.1:n.285+677T>G
|
|
XR_945642.1:n.487+677T>G
|
|
|
NM_001351263.1:c.97-9702T>G
|
NP_001338192.1:n.97-9702T>G
|
|
NM_012339.4:c.357+677T>G
|
NP_036471.1:n.357+677T>G
|
|
NR_147091.1:n.485+677T>G
|
|
|
XM_017016010.1:c.357+677T>G
|
XP_016871499.1:n.357+677T>G
|
|
XR_001747072.1:n.488+677T>G
|
|
|
XR_001747073.1:n.488+677T>G
|
|
|
XR_001747074.1:n.485+677T>G
|
|
|
NM_012339.5:c.357+677T>G
MANE Select
|
NP_036471.1:n.357+677T>G
|
|
NM_001351263.2:c.97-9702T>G
|
NP_001338192.1:n.97-9702T>G
|
|
NR_147091.2:n.487+677T>G
|
|
|