|
ENST00000507260.3:n.4958C>G
|
|
|
|
ENST00000510728.6:n.1697+39C>G
|
|
|
|
ENST00000514776.3:n.181C>G
|
|
|
|
ENST00000515462.7:n.1935C>G
|
|
|
|
ENST00000626637.2:c.721+39C>G
|
ENSP00000486771.1:n.721+39C>G
|
|
|
ENST00000638648.2:c.721+39C>G
|
ENSP00000507949.1:n.721+39C>G
|
|
|
ENST00000640201.2:n.834C>G
|
|
|
|
ENST00000640752.2:n.4919+39C>G
|
|
|
|
ENST00000682067.1:c.542+39C>G
|
|
|
|
ENST00000682086.1:n.817C>G
|
|
|
|
ENST00000682373.1:c.368+39C>G
|
|
|
|
ENST00000684696.1:c.637-140C>G
|
ENSP00000507675.1:n.637-140C>G
|
|
|
ENST00000309522.8:c.709+39C>G
MANE Select
|
ENSP00000312288.4:n.709+39C>G
|
|
|
ENST00000403312.6:c.709+39C>G
|
ENSP00000385638.3:n.709+39C>G
|
|
|
ENST00000505878.4:c.886+39C>G
|
ENSP00000425952.2:n.886+39C>G
|
|
|
ENST00000514776.2:n.181C>G
|
|
|
|
ENST00000515462.6:n.1935C>G
|
|
|
|
ENST00000638559.1:c.567+39C>G
|
|
|
|
ENST00000638621.1:c.295+39C>G
|
ENSP00000491581.1:n.295+39C>G
|
|
|
ENST00000638648.1:n.860+39C>G
|
|
|
|
ENST00000639146.1:c.709+39C>G
|
ENSP00000492345.1:n.709+39C>G
|
|
|
ENST00000639335.1:c.*144+39C>G
|
ENSP00000491310.1:n.*144+39C>G
|
|
|
ENST00000639698.1:c.516+4236C>G
|
ENSP00000492420.1:n.516+4236C>G
|
|
|
ENST00000639784.1:c.373+4236C>G
|
|
|
|
ENST00000640048.1:c.681+39C>G
|
ENSP00000492009.1:n.681+39C>G
|
|
|
ENST00000640060.1:c.*804+39C>G
|
ENSP00000492734.1:n.*804+39C>G
|
|
|
ENST00000640201.1:n.703C>G
|
|
|
|
ENST00000640752.1:n.4912+39C>G
|
|
|
|
ENST00000309522.7:c.709+39C>G
|
ENSP00000312288.3:n.709+39C>G
|
|
|
ENST00000403312.5:c.886+39C>G
|
ENSP00000385638.2:n.886+39C>G
|
|
|
ENST00000505878.3:c.721+39C>G
|
ENSP00000425952.1:n.721+39C>G
|
|
|
ENST00000507260.1:n.448C>G
|
|
|
|
ENST00000510728.5:n.249+39C>G
|
|
|
|
ENST00000515462.5:n.85C>G
|
|
|
|
ENST00000603302.5:c.709+39C>G
|
ENSP00000474560.1:n.709+39C>G
|
|
|
ENST00000626637.1:c.721+39C>G
|
ENSP00000486771.1:n.721+39C>G
|
|
|
NM_001184705.2:c.709+39C>G
|
NP_001171634.2:n.709+39C>G
|
|
|
NM_005327.4:c.709+39C>G
|
NP_005318.3:n.709+39C>G
|
|
|
XM_005262972.1:c.721+39C>G
|
XP_005263029.1:n.721+39C>G
|
|
|
XR_938726.1:n.897C>G
|
|
|
|
NM_001331027.1:c.721+39C>G
|
NP_001317956.1:n.721+39C>G
|
|
|
XR_001741214.2:n.803+39C>G
|
|
|
|
XR_002959727.1:n.842C>G
|
|
|
|
NM_001184705.3:c.709+39C>G
|
NP_001171634.2:n.709+39C>G
|
|
|
NM_005327.7:c.709+39C>G
MANE Select
|
NP_005318.6:n.709+39C>G
|
|
|
NM_001184705.4:c.709+39C>G
|
NP_001171634.3:n.709+39C>G
|
|
|
NM_001331027.2:c.721+39C>G
|
NP_001317956.2:n.721+39C>G
|
|
