ENST00000353578.9:c.4574T>C
|
ENSP00000315873.4:p.Phe1525Ser
|
|
ENST00000295550.9:c.5192T>C
MANE Select
|
ENSP00000295550.4:p.Phe1731Ser
|
|
ENST00000295550.8:c.5192T>C
|
ENSP00000295550.4:p.Phe1731Ser
|
|
ENST00000347401.7:c.3371T>C
|
ENSP00000315609.4:p.Phe1124Ser
|
|
ENST00000353578.8:c.4574T>C
|
ENSP00000315873.4:p.Phe1525Ser
|
|
ENST00000409809.5:c.4574T>C
|
ENSP00000386844.1:p.Phe1525Ser
|
|
ENST00000472056.5:c.3371T>C
|
ENSP00000418285.1:p.Phe1124Ser
|
|
NM_004369.3:c.5192T>C , LRG_473t1:c.5192T>C
|
NP_004360.2:p.Phe1731Ser
|
|
NM_057166.4:c.3371T>C
|
NP_476507.3:p.Phe1124Ser
|
|
NM_057167.3:c.4574T>C
|
NP_476508.2:p.Phe1525Ser
|
|
XM_005246065.1:c.4592T>C
|
XP_005246122.1:p.Phe1531Ser
|
|
XM_005246066.1:c.3971T>C
|
XP_005246123.1:p.Phe1324Ser
|
|
XM_006712253.1:c.4691T>C
|
XP_006712316.1:p.Phe1564Ser
|
|
XM_011510574.1:c.5189T>C
|
XP_011508876.1:p.Phe1730Ser
|
|
XM_011510575.1:c.2786T>C
|
XP_011508877.1:p.Phe929Ser
|
|
XM_017003304.1:c.2786T>C
|
XP_016858793.1:p.Phe929Ser
|
|
XM_024452684.1:c.3971T>C
|
XP_024308452.1:p.Phe1324Ser
|
|
NM_004369.4:c.5192T>C
MANE Select
|
NP_004360.2:p.Phe1731Ser
|
|
NM_057166.5:c.3371T>C
|
NP_476507.3:p.Phe1124Ser
|
|
NM_057167.4:c.4574T>C
|
NP_476508.2:p.Phe1525Ser
|
|