ENST00000478003.2:n.1902G>C
|
|
|
ENST00000682276.1:n.1519G>C
|
|
|
ENST00000682892.1:c.1621G>C
|
ENSP00000507214.1:p.Ala541Pro
|
|
ENST00000682952.1:n.1713G>C
|
|
|
ENST00000684455.1:c.1287G>C
|
|
|
ENST00000684642.1:c.1471G>C
|
ENSP00000507355.1:p.Ala491Pro
|
|
ENST00000684740.1:n.2252G>C
|
|
|
ENST00000303236.9:c.2074G>C
MANE Select
|
ENSP00000307235.3:p.Ala692Pro
|
|
ENST00000652099.1:c.2268G>C
|
|
|
ENST00000652736.1:n.1950G>C
|
|
|
ENST00000303236.7:c.2074G>C
|
ENSP00000307235.3:p.Ala692Pro
|
|
ENST00000415570.1:c.1711G>C
|
ENSP00000412076.1:p.Ala571Pro
|
|
ENST00000419748.5:c.1621G>C
|
ENSP00000408325.1:p.Ala541Pro
|
|
ENST00000478003.1:n.640G>C
|
|
|
NM_001313915.1:c.1621G>C
|
NP_001300844.1:p.Ala541Pro
|
|
NM_004836.5:c.2074G>C
|
NP_004827.4:p.Ala692Pro
|
|
NM_004836.6:c.2074G>C
|
NP_004827.4:p.Ala692Pro
|
|
NR_110236.1:n.1546C>G
|
|
|
XM_005264649.3:c.1390G>C
|
XP_005264706.1:p.Ala464Pro
|
|
XR_939749.1:n.2353G>C
|
|
|
XM_017005376.2:c.1390G>C
|
XP_016860865.1:p.Ala464Pro
|
|
NM_004836.7:c.2074G>C
MANE Select
|
NP_004827.4:p.Ala692Pro
|
|
NM_001313915.2:c.1621G>C
|
NP_001300844.1:p.Ala541Pro
|
|