|
NM_004370.6:c.43G>T
MANE Select
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NP_004361.3:p.Ala15Ser
|
|
ENST00000322507.13:c.43G>T
MANE Select
|
ENSP00000325146.8:p.Ala15Ser
|
|
NM_004370.5:c.43G>T
|
NP_004361.3:p.Ala15Ser
|
|
NM_080645.2:c.43G>T
|
NP_542376.2:p.Ala15Ser
|
|
NM_080645.3:c.43G>T
|
NP_542376.2:p.Ala15Ser
|
|
ENST00000322507.12:c.43G>T
|
ENSP00000325146.8:p.Ala15Ser
|
|
ENST00000345356.10:c.43G>T
|
ENSP00000305147.9:p.Ala15Ser
|
|
ENST00000416123.6:c.43G>T
|
ENSP00000412864.2:p.Ala15Ser
|
|
ENST00000483888.6:c.43G>T
|
ENSP00000421216.1:p.Ala15Ser
|
|
ENST00000615798.4:c.-3525G>T
|
ENSP00000483232.1:n.-3525G>T
|
|
ENST00000680102.1:n.569G>T
|
|
|
XM_011535434.1:c.43G>T
|
XP_011533736.1:p.Ala15Ser
|
|
XM_011535435.1:c.43G>T
|
XP_011533737.1:p.Ala15Ser
|
|
XM_011535436.1:c.43G>T
|
XP_011533738.1:p.Ala15Ser
|
|
XM_011535436.2:c.43G>T
|
XP_011533738.1:p.Ala15Ser
|