ENST00000347401.8:c.1610+1253G>T
|
|
|
ENST00000353578.9:c.8355G>T
|
ENSP00000315873.4:p.Met2785Ile
|
|
ENST00000682957.1:c.1100G>T
|
|
|
ENST00000295550.9:c.8973G>T
MANE Select
|
ENSP00000295550.4:p.Met2991Ile
|
|
ENST00000295550.8:c.8973G>T
|
ENSP00000295550.4:p.Met2991Ile
|
|
ENST00000347401.7:c.7149G>T
|
ENSP00000315609.4:p.Met2383Ile
|
|
ENST00000353578.8:c.8355G>T
|
ENSP00000315873.4:p.Met2785Ile
|
|
ENST00000409809.5:c.8355G>T
|
ENSP00000386844.1:p.Met2785Ile
|
|
ENST00000472056.5:c.7152G>T
|
ENSP00000418285.1:p.Met2384Ile
|
|
ENST00000491769.1:n.5415G>T
|
|
|
NM_004369.3:c.8973G>T , LRG_473t1:c.8973G>T
|
NP_004360.2:p.Met2991Ile
|
|
NM_057166.4:c.7152G>T
|
NP_476507.3:p.Met2384Ile
|
|
NM_057167.3:c.8355G>T
|
NP_476508.2:p.Met2785Ile
|
|
XM_005246065.1:c.8373G>T
|
XP_005246122.1:p.Met2791Ile
|
|
XM_005246066.1:c.7752G>T
|
XP_005246123.1:p.Met2584Ile
|
|
XM_006712253.1:c.8472G>T
|
XP_006712316.1:p.Met2824Ile
|
|
XM_011510574.1:c.8970G>T
|
XP_011508876.1:p.Met2990Ile
|
|
XM_011510575.1:c.6567G>T
|
XP_011508877.1:p.Met2189Ile
|
|
XM_017003304.1:c.6567G>T
|
XP_016858793.1:p.Met2189Ile
|
|
XM_024452684.1:c.7752G>T
|
XP_024308452.1:p.Met2584Ile
|
|
NM_004369.4:c.8973G>T
MANE Select
|
NP_004360.2:p.Met2991Ile
|
|
NM_057166.5:c.7152G>T
|
NP_476507.3:p.Met2384Ile
|
|
NM_057167.4:c.8355G>T
|
NP_476508.2:p.Met2785Ile
|
|