ENST00000347401.8:c.1239G>A
|
|
|
ENST00000353578.9:c.7976G>A
|
ENSP00000315873.4:p.Ser2659Asn
|
|
ENST00000682957.1:c.721G>A
|
|
|
ENST00000684508.1:n.861G>A
|
|
|
ENST00000295550.9:c.8594G>A
MANE Select
|
ENSP00000295550.4:p.Ser2865Asn
|
|
ENST00000295550.8:c.8594G>A
|
ENSP00000295550.4:p.Ser2865Asn
|
|
ENST00000347401.7:c.6770G>A
|
ENSP00000315609.4:p.Ser2257Asn
|
|
ENST00000353578.8:c.7976G>A
|
ENSP00000315873.4:p.Ser2659Asn
|
|
ENST00000409809.5:c.7976G>A
|
ENSP00000386844.1:p.Ser2659Asn
|
|
ENST00000472056.5:c.6773G>A
|
ENSP00000418285.1:p.Ser2258Asn
|
|
ENST00000491769.1:n.5036G>A
|
|
|
NM_004369.3:c.8594G>A , LRG_473t1:c.8594G>A
|
NP_004360.2:p.Ser2865Asn
|
|
NM_057166.4:c.6773G>A
|
NP_476507.3:p.Ser2258Asn
|
|
NM_057167.3:c.7976G>A
|
NP_476508.2:p.Ser2659Asn
|
|
XM_005246065.1:c.7994G>A
|
XP_005246122.1:p.Ser2665Asn
|
|
XM_005246066.1:c.7373G>A
|
XP_005246123.1:p.Ser2458Asn
|
|
XM_006712253.1:c.8093G>A
|
XP_006712316.1:p.Ser2698Asn
|
|
XM_011510574.1:c.8591G>A
|
XP_011508876.1:p.Ser2864Asn
|
|
XM_011510575.1:c.6188G>A
|
XP_011508877.1:p.Ser2063Asn
|
|
XM_017003304.1:c.6188G>A
|
XP_016858793.1:p.Ser2063Asn
|
|
XM_024452684.1:c.7373G>A
|
XP_024308452.1:p.Ser2458Asn
|
|
NM_004369.4:c.8594G>A
MANE Select
|
NP_004360.2:p.Ser2865Asn
|
|
NM_057166.5:c.6773G>A
|
NP_476507.3:p.Ser2258Asn
|
|
NM_057167.4:c.7976G>A
|
NP_476508.2:p.Ser2659Asn
|
|