ENST00000361915.8:c.*301G>C
MANE Select
|
ENSP00000355106.3:n.*301G>C
|
|
ENST00000637337.1:n.5111G>C
|
|
|
ENST00000294724.8:c.*301G>C
|
ENSP00000294724.4:n.*301G>C
|
|
ENST00000361302.7:c.*301G>C
|
ENSP00000354971.3:n.*301G>C
|
|
ENST00000361522.4:c.*301G>C
|
ENSP00000354635.4:n.*301G>C
|
|
ENST00000361915.7:c.*301G>C
|
ENSP00000355106.3:n.*301G>C
|
|
ENST00000370161.6:c.4852G>C
|
ENSP00000359180.2:n.4852G>C
|
|
ENST00000370163.7:c.*301G>C
|
ENSP00000359182.3:n.*301G>C
|
|
ENST00000370165.7:c.*301G>C
|
ENSP00000359184.3:n.*301G>C
|
|
NM_000028.2:c.*301G>C
|
NP_000019.2:n.*301G>C
|
|
NM_000642.2:c.*301G>C
|
NP_000633.2:n.*301G>C
|
|
NM_000643.2:c.*301G>C
|
NP_000634.2:n.*301G>C
|
|
NM_000644.2:c.*301G>C
|
NP_000635.2:n.*301G>C
|
|
NM_000645.2:c.*301G>C
|
NP_000636.2:n.*301G>C
|
|
NM_000646.2:c.*301G>C
|
NP_000637.2:n.*301G>C
|
|
XM_005270557.1:c.*301G>C
|
XP_005270614.1:n.*301G>C
|
|
XR_947626.1:n.1317+2286C>G
|
|
|
XR_947627.1:n.1206+2286C>G
|
|
|
XR_947628.1:n.1311+2286C>G
|
|
|
XR_947630.1:n.1249+2286C>G
|
|
|
XR_947632.1:n.1135+2286C>G
|
|
|
XR_947633.1:n.1246+2286C>G
|
|
|
XR_947634.1:n.660+2286C>G
|
|
|
XR_947635.1:n.728+2286C>G
|
|
|
XM_005270557.2:c.*301G>C
|
XP_005270614.1:n.*301G>C
|
|
XM_017000501.2:c.*301G>C
|
XP_016855990.1:n.*301G>C
|
|
NM_000642.3:c.*301G>C
MANE Select
|
NP_000633.2:n.*301G>C
|
|