ENST00000347401.8:c.1553C>A
|
|
|
ENST00000353578.9:c.8290C>A
|
ENSP00000315873.4:p.Pro2764Thr
|
|
ENST00000682957.1:c.1035C>A
|
|
|
ENST00000684508.1:n.1175C>A
|
|
|
ENST00000295550.9:c.8908C>A
MANE Select
|
ENSP00000295550.4:p.Pro2970Thr
|
|
ENST00000295550.8:c.8908C>A
|
ENSP00000295550.4:p.Pro2970Thr
|
|
ENST00000347401.7:c.7084C>A
|
ENSP00000315609.4:p.Pro2362Thr
|
|
ENST00000353578.8:c.8290C>A
|
ENSP00000315873.4:p.Pro2764Thr
|
|
ENST00000409809.5:c.8290C>A
|
ENSP00000386844.1:p.Pro2764Thr
|
|
ENST00000472056.5:c.7087C>A
|
ENSP00000418285.1:p.Pro2363Thr
|
|
ENST00000491769.1:n.5350C>A
|
|
|
NM_004369.3:c.8908C>A , LRG_473t1:c.8908C>A
|
NP_004360.2:p.Pro2970Thr
|
|
NM_057166.4:c.7087C>A
|
NP_476507.3:p.Pro2363Thr
|
|
NM_057167.3:c.8290C>A
|
NP_476508.2:p.Pro2764Thr
|
|
XM_005246065.1:c.8308C>A
|
XP_005246122.1:p.Pro2770Thr
|
|
XM_005246066.1:c.7687C>A
|
XP_005246123.1:p.Pro2563Thr
|
|
XM_006712253.1:c.8407C>A
|
XP_006712316.1:p.Pro2803Thr
|
|
XM_011510574.1:c.8905C>A
|
XP_011508876.1:p.Pro2969Thr
|
|
XM_011510575.1:c.6502C>A
|
XP_011508877.1:p.Pro2168Thr
|
|
XM_017003304.1:c.6502C>A
|
XP_016858793.1:p.Pro2168Thr
|
|
XM_024452684.1:c.7687C>A
|
XP_024308452.1:p.Pro2563Thr
|
|
NM_004369.4:c.8908C>A
MANE Select
|
NP_004360.2:p.Pro2970Thr
|
|
NM_057166.5:c.7087C>A
|
NP_476507.3:p.Pro2363Thr
|
|
NM_057167.4:c.8290C>A
|
NP_476508.2:p.Pro2764Thr
|
|