ENST00000347401.8:c.1610+1254T=
|
|
|
ENST00000353578.9:c.8356T=
|
ENSP00000315873.4:p.Ser2786=
|
|
ENST00000682957.1:c.1101T=
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|
|
ENST00000295550.9:c.8974T=
MANE Select
|
ENSP00000295550.4:p.Ser2992=
|
|
ENST00000295550.8:c.8974T=
|
ENSP00000295550.4:p.Ser2992=
|
|
ENST00000347401.7:c.7150T=
|
ENSP00000315609.4:p.Ser2384=
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|
ENST00000353578.8:c.8356T=
|
ENSP00000315873.4:p.Ser2786=
|
|
ENST00000409809.5:c.8356T=
|
ENSP00000386844.1:p.Ser2786=
|
|
ENST00000472056.5:c.7153T=
|
ENSP00000418285.1:p.Ser2385=
|
|
ENST00000491769.1:n.5416T=
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|
|
NM_004369.3:c.8974T= , LRG_473t1:c.8974T=
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NP_004360.2:p.Ser2992=
|
|
NM_057166.4:c.7153T=
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NP_476507.3:p.Ser2385=
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|
NM_057167.3:c.8356T=
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NP_476508.2:p.Ser2786=
|
|
XM_005246065.1:c.8374T=
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XP_005246122.1:p.Ser2792=
|
|
XM_005246066.1:c.7753T=
|
XP_005246123.1:p.Ser2585=
|
|
XM_006712253.1:c.8473T=
|
XP_006712316.1:p.Ser2825=
|
|
XM_011510574.1:c.8971T=
|
XP_011508876.1:p.Ser2991=
|
|
XM_011510575.1:c.6568T=
|
XP_011508877.1:p.Ser2190=
|
|
XM_017003304.1:c.6568T=
|
XP_016858793.1:p.Ser2190=
|
|
XM_024452684.1:c.7753T=
|
XP_024308452.1:p.Ser2585=
|
|
NM_004369.4:c.8974T=
MANE Select
|
NP_004360.2:p.Ser2992=
|
|
NM_057166.5:c.7153T=
|
NP_476507.3:p.Ser2385=
|
|
NM_057167.4:c.8356T=
|
NP_476508.2:p.Ser2786=
|
|