ENST00000347401.8:c.1235T>G
|
|
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ENST00000353578.9:c.7972T>G
|
ENSP00000315873.4:p.Ser2658Ala
|
|
ENST00000682957.1:c.717T>G
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|
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ENST00000684508.1:n.857T>G
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|
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ENST00000295550.9:c.8590T>G
MANE Select
|
ENSP00000295550.4:p.Ser2864Ala
|
|
ENST00000295550.8:c.8590T>G
|
ENSP00000295550.4:p.Ser2864Ala
|
|
ENST00000347401.7:c.6766T>G
|
ENSP00000315609.4:p.Ser2256Ala
|
|
ENST00000353578.8:c.7972T>G
|
ENSP00000315873.4:p.Ser2658Ala
|
|
ENST00000409809.5:c.7972T>G
|
ENSP00000386844.1:p.Ser2658Ala
|
|
ENST00000472056.5:c.6769T>G
|
ENSP00000418285.1:p.Ser2257Ala
|
|
ENST00000491769.1:n.5032T>G
|
|
|
NM_004369.3:c.8590T>G , LRG_473t1:c.8590T>G
|
NP_004360.2:p.Ser2864Ala
|
|
NM_057166.4:c.6769T>G
|
NP_476507.3:p.Ser2257Ala
|
|
NM_057167.3:c.7972T>G
|
NP_476508.2:p.Ser2658Ala
|
|
XM_005246065.1:c.7990T>G
|
XP_005246122.1:p.Ser2664Ala
|
|
XM_005246066.1:c.7369T>G
|
XP_005246123.1:p.Ser2457Ala
|
|
XM_006712253.1:c.8089T>G
|
XP_006712316.1:p.Ser2697Ala
|
|
XM_011510574.1:c.8587T>G
|
XP_011508876.1:p.Ser2863Ala
|
|
XM_011510575.1:c.6184T>G
|
XP_011508877.1:p.Ser2062Ala
|
|
XM_017003304.1:c.6184T>G
|
XP_016858793.1:p.Ser2062Ala
|
|
XM_024452684.1:c.7369T>G
|
XP_024308452.1:p.Ser2457Ala
|
|
NM_004369.4:c.8590T>G
MANE Select
|
NP_004360.2:p.Ser2864Ala
|
|
NM_057166.5:c.6769T>G
|
NP_476507.3:p.Ser2257Ala
|
|
NM_057167.4:c.7972T>G
|
NP_476508.2:p.Ser2658Ala
|
|